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Life Science Specialists

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VIEW OUR SPECIALISMS

TESTIMONIALS

  • “I had the pleasure of working with Hamlyn Williams on a very tough search. They are consummate professionals, a reliable and knowledgeable recruiter. Being very responsive, they took the time to understand the requirements of the position and asking the right questions. They were adaptable, continuously finetuning the search, and was very thorough in their screening process. They continued to recruit for the position even after the right candidate had been identified, and up to the point where an offer was extended, something very few agency recruiters tend to do. They are among my most dependable recruitment partners, and I would enjoy the opportunity to work with them again.”

    Kavitha Manley
    Kavitha Manley

    Associate Director, Talent Acquisition

WE ARE GLOBAL


WE CAN SUPPORT YOUR BUSINESS AS IT GROWS

We operate globally with 7 offices across the EMEA, N.America and APAC regions.

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RESEARCH & DEVELOPMENT

HW Life Sciences places leading professionals within the Biotech, Pharmaceutical, Medical Device and Medical technology industries at the research  and development phase of the life cycle.

PRODUCTION

HW Life Sciences places industry leading professionals within Biotech, Pharmaceutical, Medical Device and Medical Technology industries at the production phase of the development life cycle.

COMMERCIALIZATION

HW Life Sciences places industry leading professionals within Biotech, Pharmaceutical, Medical Device and Medical Technology industries post product approval to commercialization. 

OUR LATEST JOBS


  • Financial Services and Banking

  • Life Sciences

  • Technology

  • Healthcare
  • Regulatory Compliance Analyst

    Los Angeles

    An Asset Management client in the Los Angeles area is looking for an experienced RIA Regulatory Compliance professional to join its team. This role will sit within an existing team located in L.A but will also support and work with Compliance professional across the world in multiple locations. You will report directly in to the Chief Compliance Officer and be required to primarily support the administration of the Firm's Compliance Monitoring Program. Responsibilities: Assist non-US offices with various aspects of their local programs, when required Help to analyze new regulations, alerts, sample exam lists, enforcement actions Assist in administration of regulatory examinations when required The CMP role provided assurance on day-to-day operations which is the core of the group’s regulatory mission Other duties as required by the CCO Requirements: 2+ years’ worth of Regulatory Compliance experience, in an RIA setting or at an Asset Management firm The ability to administer the Compliance Monitoring Program, but also understanding the policy rationale behind the tests and applying that knowledge to the tests or revising the tests as needed Bachelor’s Degree If this opportunity interests you, please get in touch!

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  • Model Validation Senior Analyst

    Los Angeles

    A banking client in Los Angeles is looking for a model validation professional to join its Model Risk Management team. In this role, this individual will be expected to lead the effort to perform independent validations on statistical and financial models across different business-area models. Responsibilities: Complete procedures of material model components including: Assess and test the conceptual soundness Evaluate model assumptions and data integrity for accuracy and reasonability Test model numerical, statistical, and/or computational accuracy Perform outcomes analysis including but not limited to back-testing, scenario testing, and sensitivity testing Review model governance and control process; and assess the suitability and implementation of vendor models Build benchmark or challenge models when necessary, using the best-practice approach in the appropriate areas Write and present in-depth model validation reports and provide value-added recommendations to model owners and developers Assess and test model performance and maintenance, i.e. correct implementation, limiting behaving, and response to stress/extreme input condition-stress testing Interprets model validation test results and establish and assess the required action plans with model owners and developers Gain in-depth understanding of the available data sources and help build an effective data governance framework Requirements: 4-10 years' worth of experience with model validation or development Prior experience developing/validating of the following (2 or more preferred): Quantitative Risk Management (QRM) CoStar Compass Moody’s RiskCalc (or other Moody’s models such as Impairment Studio, GCorr, ECCL) Anti-Money Laundering Models CECL Models Enterprise Stress Testing models Experience in designing tests, model outcomes analysis, scenario analysis, sensitivity analysis, and back-testing Knowledge of model risk management and associated regulatory requirements such as SR11-7/OCC2011-12 and ideally proficient in SAS, R, Python, VBA, SQL programming If this opportunity interest you, please get in touch to epxlore further!

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  • Senior KYC Analyst

    Athens

    Hamlyn Williams is working with one of the fastest-growing global FinTech's, and we’re looking for a highly organized, diligent and proactive Senior KYC Analyst to support their Greek business. You’ll be responsible for the KYC analysis and documentation of new and existing business and you must immediately identify suspicious activities that do not match the profile of the customer. As a Senior KYC Analyst, you will but not limited to: Ensure compliance with relevant legal and regulatory standards and internal processes and procedures Identify customers who are at higher risk due to “Red Flags” or other triggers Carry out validation of CDD tests according to the “4-eyes principle” Independently resolve issues that arise during the CDD process and adequately handle more complex cases Prepare and manage data for internal and external audits Monitor activities of existing customers and update relevant data As a Senior KYC Analyst, you will have: Minimum 5 years' experience of CDD processes and requirements, including the regulatory basis for these Advanced knowledge of red flags and AML typologies relevant to the payments and FX space in Greece Client/ customer experience, ability to liaise with Greek clients Proactive way of working and ideally first-hand work experience in a fast working environment If you are a skilled KYC specialist within the FinTech payments space, you can apply by: Selecting the Apply button below or contact Sophie Stone directly at s.stone@hamlynwilliams.com

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  • Compliance Analyst

    Detroit, MI

    A banking client of ours based in Detroit is looking for a Compliance Analyst. This position is responsible for performing federal and state statutory and regulatory compliance duties under the direct supervision of the Compliance Officer, to assist in the development and maintenance of a strong professional compliance management program and to ensure that all banking rules, regulations, and statutory requirements are met. Resposibilities include: Maintain and review policies, procedures, and practices to ensure compliance with laws and regulations. Assist with development and maintenance of the bank’s compliance and risk management programs. Assist with testing the effectiveness of the bank’s policies and procedures and overall compliance program. Assist with conduction monitoring activities of regulatory requirements within the various departments of the bank. Work with the Compliance Officer to manager any corrective actions to completion. Perform special projects as needed and manage all related files and documentation. Comply with all federal, state, and local regulatory rules and regulations governing financial institutions, as well as all company policies and procedures. Complete and pass all required regulatory compliance training as assigned. Perform other tasks which may be assigned by management. Requirements include: Bachelors degree 1+ years of relevent experience within financial services industry If you are interested in exploring this opportunity, please get in touch!

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  • Clinical Supply Manager

    Remote

    CLINCIAL SUPPLY MANAGER SCOPE Rare opportunity to contribute to the Clincal Suppyl Team of a growing biopharmaceutical company with an exciting oncology portfolio. This long-term contract position has the possibility of becoming permament for the selected candidate and offers remote flexibility. As a Clinical Supply Manager, you will oversee all aspects of supply forecast plans and drug delivery. RESPONSIBILITIES Review, interpret and implement supply forecast plans Review SOPs and protocol amendments for drug supply needs; adjust forecast as needed Create and review Pharmacy Manuals Provide instructions to sites on drug storage, usage, returns, drug accountability and temperature requirements Managed all IRT activities regarding drug supply ensuring continuous and uninterrupted drug supply to clinical sites Review and approve site-generated IRT queries Manage vendor operations supporting US and global clinical trials by working collaboratively with Clinical Operations, CMC, Regulatory, QA and Finance teams REQUIREMENTS Bachelor's degree in biology or life sciences required Advanced degree in life sciences preferred 3+ years clinical trial supply management experience required Previous oncology clinical trial experience strongly preferred Demonstrated knowledge of industry regulatory requirements, including ICH/GCP and clinical trial operations guidelines SKILLS: Excellent verbal and written communication skills Strong management skills and demonstrated team-building skills Ability to work in fast-paced environments within strict timeline My team and I are working on a number of additional opportunities for a broad portfolio of clients across the US and internationally. If this role isn't for you but you would like to explore your options in the market, I would welcome a confidential conversation at your convenience. Please contact me at (619) 350-6149 or e.mato@hamlynwilliams.com.

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  • Automation Engineer

    Maine, United States

    Automation Engineer Maine, US Hamlyn Williams are currently partnered with a leading System Integration and Engineering organisation who have a strong footprint and network in the New England region and are looking to expand their Automation team, due to a large amount of projects that have been won and that have come through. They would be looking for someone to join the project team, to work with their customers across the full project lifecycle, consulting with them whilst carrying out the work technically as well. Responsibilities include: Defining automation architecture requirements Developing detailed functional and software design specifications Programming PLC and SCADA applications Providing control systems commissioning services Troubleshoot existing control systems Experience Needed: Bachelors degree or higher Minimum of 3 years programming experience Experience with Rockwell Automation products (Controllogix, FTView). Experience with other automation platforms (Siemens S7 or DeltaV) Apply Now You can apply for this role by sending us your CV or by calling us now! James Brookes Contact: 0203 545 1103 or email j.brookes@hamlynwilliams.com. We recruit for a variety of opportunities in Life Sciences so feel free to get in touch with us to find out how we can help you. You can learn more about me by looking me up on LinkedIn. Search for James Brookes https://www.linkedin.com/in/jamesbrookeshw/

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  • Electrical Engineer

    Brussels

    Electrical Engineer Brussels Do you want to work for one of the largest pharmaceuticals companies in the world, who have one of the most exciting projects currently on the market at the moment? Hamlyn Williams are partnered with a leading Biotech company, based in Brussels, who are looking to hire an Electrical Engineer to join their Automation/E&I team on a number of exciting CAPEX projects that are going to be coming in the next few years. Experience required: Must hold an Industrial Electrical engineer diploma or equivalent. At least 10 years experience of working within the pharmaceutical environment Experience in electrical networks (High and Low Voltage) CAD software (Elec Cal and Eplans) and office automation (Office 365); The work environment in the ATEX zone is an asset Experience in design and sizing of industrial electrical installations, carrying out costing and studies related to electricity Must hold BA4/BA5 accreditation and hold a VCA cert French speaking is a MUST for this role. Apply Now You can apply for this role by sending us your CV or by calling us now! James Brookes Contact: 0203 545 1103 or email j.brookes@hamlynwilliams.com. We recruit for a variety of opportunities in Life Sciences so feel free to get in touch with us to find out how we can help you. You can learn more about me by looking me up on LinkedIn. Search for James Brookes https://www.linkedin.com/in/jamesbrookeshw/

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  • Senior Clinical Data Manager

    Cambridge

    SENIOR DATA MANAGER Our client is a midsize biotech company operating in the neurodegenerative diseases space actively hiring for a Senior Data Manager reporting directly into the Director of Data Management. The client has a deep pipeline and looking for the most exceptional individual to add to their continued success in their MA based office. Job Description: Responsible for the execution and management of the design, testing documenting and implementing of clinical database Overseeing and development of data transfer agreements between data management and external vendors Preserving data integrity while adhering to strict timelines to achieve precise and prompt regulatory submissions and publications Building and evaluating of all data and adherence to relevant processes throughout the lifecycle of clinical trials Qualifications: 5+ years experience in Data Management specifically in a pharmaceutical/biotechnology industry with leadership experience Bachelor’s degree in scientific discipline Comprehensive understanding of SDTM, CDASH and medical coding dictionaries MedDRA Proficient in Medidata Rave and other electronic data capture systems Apply here or by direct contact (646) 349-2959 l.wysocki@hamlynwilliams.com if you are interested in working with an elite pharmaceutical company.

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  • Manager

    Shenzhen

    Hamlyn Williams are looking for a highly experienced recruiter to head up our Technology team in Shenzhen. This individual will be a key part of our China expansion and our broader leadership team in the region. This person will be responsible for growing out our Technology business by building strong relationships with clients in our industry, leading from the front and delivering outstanding service into our clients. Leveraging the relationships with our current major clients in Shenzhen and around the world will also be essential. Hamlyn Williams will give you the opportunity and autonomy you need to succeed. Experience managing a team is ideal but not essential. A proven track record as a top biller is a must. If you consider yourself a proactive, sales focused, high energy, competitive, and entrepreneurial individual you will be a perfect fit for the company! Job Description • Win business and create long-lasting partnerships with new clients. • Manage relationships with existing clients and leverage our relationships with clients globally. • Transform our Technology accounts into group wide accounts. • Hit quarterly budget targets. • Hit headcount growth figures. • Day to day management of the Technology team. • Train and onboard new teammates, and provide guidance and mentorship to the entire team. Develop new hires into successful 360 conultants. • You know how to positively impact others: responsible for the performance, effort, and attitude of yourself and each team member • Lead qualification, prospecting, pipeline building & opportunity identification • Present weekly to the global team on past performance, what the team is working on, and weekly wins. Requirements • 5-10 years recruitment experience. • Proven billing record • Evidence of strong business development acumen • Fluent in English and Cantonese, Mandarin a bonus Benefits • Competitive base salary • Industry leading commission scheme • Health insurance • Company incentives including fine diners, holidays and more

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  • Software Developer - SaaS / Fintech

    Cardiff

    HW are currently working with a SaaS tech scale up business based in Cardiff, who are utilizing modern technology and machine learning to provide a new approach to sales market intelligence. The organisation are looking for a talented, enthusiastic, self-motivated, inquisitive and knowledgeable software developer to join an already established team. If you are knowledgeable, passionate about working on developing and implementing new software with exposure to SaaS development then this could be the role for you! The skilled Software Developer will be responsible for: Front End/Full Stack development Managing user-facing website Development of mobile apps The chance to develop, contributing to teams with A.I. and content generation The skilled Software Developer will need: Highly experienced in JavaScript/Angular Other coding languages such as python 3.x, MongoDB, React native, HTML a benefit. Exposure to Postgres a benefit Evidence of working across the stack Working in Agile/Scrum (desirable) Experience of Cloud based software

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  • Automation Engineer (PLC)

    Cork

    Automation Engineer – Cork 6 months contract (possibility for extension) Hamlyn Williams is currently working with one of the worlds leading biotechnology organisations at the moment, based in Cork, who are looking to hire an experienced Automation Engineer on a rolling 6 month contract basis, due to an increase in demand and project work on site. This has the potential be extended for another 12 months at least, providing longevity and financial opportunities. Experience required: 5+ years (absolute minimum) of hands on practical industrial automation experience, preferable in high speed packaging environments. Siemens PLC knowledge is essential – Full project lifecycle experience Ideally someone with good level of knowledge on Elau PLCs and Rockwell systems also. Experience with vision systems (ideally Cognex) and industrial printers. Strong IT background. Understands industrial networking, Windows and Linux based OS and SCADA / HMI’s. Life science industry experience is a must. Would consider Medical Device, Pharma or Biotech. Experience working to GMP standards. Apply Now You can apply for this role by sending us your CV or by calling us now! James Brookes Contact: 0203 545 1103 or email j.brookes@hamlynwilliams.com. We recruit for a variety of opportunities in Life Sciences so feel free to get in touch with us to find out how we can help you. You can learn more about me by looking me up on LinkedIn. Search for James Brookes https://www.linkedin.com/in/jamesbrookeshw/

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  • Director - Information Security

    Hong Kong

    The role: The successful candidate will assume the role of Cyber Operations Manager on the company’s Cyber Operations and Defence team. You will take responsibility for the overall operations relating to Information and Data security, including the maintenance and monitoring of all IT Security solutions. In addition to day-to-day operations you will contribute to the strategic vision, scoping of requirements, system design, implementation, change management, incident response, budgetary control and adherence to regulations and legal requirements. Manage teams and resources to ensure that IT Security Operations is delivering secure and robust services across the group. Lead the definition and scoping of IT Security requirements, creation and execution of IT Security related strategies and the improvement of reliability and security across the company’s IT systems, projects and data. Define OPEX improvement and CAPEX items for budget forecasting and planning relating to IT Security Operations and Maintenance. Oversight of vulnerability audits, penetration tests and forensic IT audits. Management of partners, key stakeholders and third-party vendors. Ensuring that IT Security Operational SLAs, protocols, methodologies and procedures are implemented successfully. Review and optimise the performance of security telemetry and infrastructure detection capability. Lead the investigation and resolution of security issues across the group. Work with partners across the business to ensure operational compliance with information security standards and practices. Requirements: 10+ years’ experience in information security, technology and risk management and programme delivery Industry-recognised certification(s) in information security or equivalent (CRISC, CISA, CISM, CISSP, etc.) Substantial team leadership experience Fluent English, oral and written. Cantonese and/or Mandarin would be advantageous but not essential.

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JOIN THE CONVERSATION

CQV Engineers join the conversation online! Our LinkedIn group is a place for you to talk about related subjects, hot topics in the industry or a place to discuss certain problems that have arisen in your day to day work, as well as brand new job opportunities that arise.

Engineers globally are welcome!

ABOUT US

Hamlyn Williams Life Sciences was established in January 2016 to respond to the shortage of Regulatory Professionals across the Life Sciences out of our New York Office by now Director Alex McGarel.

Since then we have grown to a global team of over 20 consultants spread across our seven offices servicing the most innovative Pharmaceutical, Biotech, Medical Technology and Medical Device organizations in the hope of playing our part and providing the best talent enabling our clients to continue to innovate in the space and bring therapies to the global consumer in the fight to diagnose, treat, cure & ultimately prevent Human Disease.

Our specialist consultants work with the best talent across the Research, Regulatory, Production & Commercialization  stages of the drug development life cycle.


Our launch of Hamlyn Williams Life Sciences is an exciting step for our truly global business . If you have enquiries regarding opportunities or partnering to grow your team please reach out to our Head of US Life Sciences Alex McGarel or Head of EMEA James Brookes.

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