Manager Quality Control - Biochemistry Labs Jobs

New

Manager Quality Control - HPLC Labs

Lead the HPLC Labs during the 2nd shift —ensuring compliant, accurate testing an...

Location

United States , Juncos

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree
OR Master’s degree and 3 years of Manufacturing Support, Quality Control and/or Laboratory experience
OR Bachelor’s degree and 5 years of Manufacturing Support, Quality Control and/or Laboratory experience
OR Associate’s degree and 10 years of Manufacturing Support, Quality Control and/or Laboratory experience
OR High school diploma / GED and 12 years of Manufacturing Support, Quality Control and/or Laboratory experience
Experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation of resources
Educational background in Life Sciences, Chemistry, Biochemistry, or related fields
Experience in Quality and/or Biochemistry Laboratory operations within a GMP environment, preferably in HPLC testing
Strong knowledge of analytical techniques such as HPLC
Familiarity with laboratory systems such as LIMS, LMES, CIMS, and Empower for HPLC data management

Job Responsibility

Lead and develop a successful QC team, fostering a culture of safety, compliance, and continuous improvement
Oversee daily QC operations to ensure timely, accurate, and reliable testing aligned with production schedules
Serve as the QC subject matter expert during audits and inspections, ensuring inspection readiness
Provide technical guidance and troubleshooting support for complex assays and testing issues
Drive training initiatives and ensure team members are appropriately cross-trained for operational flexibility
Monitor assay results and documentation to ensure compliance with cGMP, SOPs, and regulatory standards
Communicate clear expectations on safety, quality, and compliance, addressing discrepancies promptly
Organize and prioritize team tasks based on impact and deadlines, adjusting as needed to meet changing requirements
Use data and dashboards to monitor QC performance metrics, identify trends, and implement improvements
Collaborate with cross-functional stakeholders to align QC activities with broader site and organizational goals

What we offer

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental & vision coverage, and life & disability insurance
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans and an annual site shutdown
Flexible work models where possible

Fulltime

New

Associate Quality Control (Analytical)

Amgen is one of the world’s leading independent biotechnology companies. For ove...

Location

Singapore , Tuas

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Bachelor’s Degree in Chemistry, Biochemistry, Life Science or related technological field and 2 years of directly related experience
Associate’s Degree in Chemistry, Biochemistry, Life Science or related technological field and 4 years of directly related experience
High School Diploma in Chemistry, Biochemistry, Life Science or related technological field / GED and 6 years of directly related experience
1-2 years of relevant laboratory experience in the commercial manufacturing environment within the pharmaceutical or biopharmaceutical industry and analytical testing experience preferred
Knowledge and understanding of GMP pharmaceutical production, pharmaceutical plant operation and associated testing methods
Experience with Quality Control testing and laboratory operations for common testing methods and equipment (e.g. including but not limited to UPLC, HPLC, LC-MS, GC-HS, LOD, Auto-titration, KF, Optical Rotation, wet chemistry, FT-IR, pH, conductivity, TOC, Potency, ELISA, Capillary Electrophoresis, DNA Testing)
Good communication skills (technical writing and verbal communication/ presentation)
Interact effectively with variety of communication and working styles and ability to work well in teams
Ability to manage multiple simultaneous activities in a rapidly changing environment
Problem solving skills and troubleshooting skills with the ability to apply logic and assess data to reach decisions and solutions related to compliance and product quality

Job Responsibility

Perform analytical testing of in-process control, drug substance intermediate, final release, stability and plant cleaning samples in a GMP pharmaceutical environment
Support laboratory operations including but not limited to equipment qualification, calibration, cleaning and maintenance, reagent/ buffer preparation
Responsible for maintenance of chemicals and consumables inventory
Ensure proper handling, storage, disposal of all chemicals used in the lab
Responsible for laboratory housekeeping and document archival duties
Participate in laboratory investigations and assist in timely closure of investigations, CAPAs and deviations
Participate in method verification and method validation/ transfer for new product introduction (when required)
Perform review of laboratory data/ records
Assist in SOP/ protocol/ report writing
Assist in periodic review of laboratory procedures and risk assessment

What we offer

Vast opportunities to learn and move up and across our global organization
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

Fulltime

Senior Director, Quality Control Analytical Sciences

We are seeking a Senior Director, Quality Control (QC) Analytical Sciences, to l...

Location

Salary:

245000.00 - 260000.00 USD / Year

Apogee Therapeutics

Expiration Date

Until further notice

Requirements

PhD in relevant discipline (e.g., analytical biochemistry or relevant field)
15+ years of QC experience with complex biologics, particularly monoclonal antibodies, spanning late-stage development and commercialization
Proven people leader with a growth mindset, willing to learn from others, and dedication to promoting a psychologically safe environment
Excellent communicator with an ability to present to and be understood by a variety of stakeholders and tailor message accordingly
Experience with regulatory filing preparation and messaging across global jurisdictions
Deep knowledge and understanding of relevant global regulatory guidance and requirements
Ability to keep pace with a fast-moving organization
Availability to participate in calls across multiple international time zones
Successfully exhibit Apogee’s C.O.R.E. values: Caring, Original, Resilient and Egoless
Ability and willingness to travel up to 30%

Job Responsibility

Lead QC Analytical Sciences team, responsible for QC activities for all pipeline programs including strategies for phase-appropriate method qualification, validation, and transfer for drug substance, drug product, and drug-device combination testing
in-process/release/stability testing
specification justification and maintenance
shelf-life management
and critical documentation
Partner with new and existing external QC testing labs and CDMOs, managing relationships and all relevant activities in collaboration with TechOps Program Management, Quality Assurance, and Manufacturing
Develop analytical regulatory strategies and prepare relevant Module 3 regulatory documents
Contribute to a mature QC infrastructure, implementing processes and procedures to support the development of therapeutic candidates in a GMP-compliant manner
Monitor data trends, troubleshoot QC method performance, and investigate OOT/OOS results

What we offer

Market competitive compensation and benefits package, including base salary, performance bonus, equity grant opportunities, health, welfare & retirement benefits
three weeks PTO, two one-week company-wide shutdowns a year and dedicated paid sick leave
Commitment to growing you professionally and providing access to resources to further your development
Apogee offers regular all team, in-person meetings to build relationships and problem solve

Fulltime

Quality Control Analyst

Are you a Quality Control Analyst interested in joining a big global pharmaceuti...

Location

Greece , Schimatari

Salary:

Not provided

Randstad

Expiration Date

December 30, 2025

Requirements

Ensuring accuracy in documentation and test results
Proficiency in laboratory software and data management
Ability to clearly report and interpret test results
Bachelor's degree in chemistry, biochemistry, pharmacy, or a related field
Familiarity with lab techniques like HPLC, GC, and spectroscopy
Understanding of Good Manufacturing Practices and regulatory guidelines
Ability to conduct precise and accurate testing

Job Responsibility

GLP document preparation e.g. SOPs, Specification and Method of Analysis, Certificate of Analysis etc.
Good documentation practices and record keeping of all GMP documents / logs. (RM, PM, IP, FP sampling and testing)
Sampling and testing: RM, PM, FP and stability samples
Stability sample management and stability protocol preparation
Daily calibration and verification checks for QC instruments
Impurity and standard managements
Daily monitoring of data loggers and recording
Management of HPLC/GC Columns
Procurement of Laboratory chemicals & consumables

New

Labourer

Labourer required for a start in Windsford. Randstad required a Labourer in Wind...

Location

United Kingdom , Winsford

Salary:

17.00 GBP / Hour

Randstad

Expiration Date

January 01, 2026

Requirements

Must have 2 references from previous employer
Must have a valid in date CSCS
Ability to follow job and safety instructions

Job Responsibility

Moving materials around site
Putting up fencing
Digging holes for fence posts
Helping out skilled tradesmen on a new build residential site

New

Mobile AC Engineer

We're hiring an experienced, qualified Mobile A/C Engineer to join our establish...

Location

United Kingdom , Swindon

Salary:

42000.00 GBP / Year

Randstad

Expiration Date

January 13, 2026

Requirements

NVQ Level 2 (min) Air-conditioning and Refrigeration
F Gas 2079/2089 qualified
Proven commercial experience in Building Services/FM
17th Edition is highly desired
Candidates must be eligible to live and work in the UK

Job Responsibility

Maintaining a portfolio of commercial properties
Maintenance role covering PPMs, breakdowns, and servicing on diverse commercial systems including VRV/VRFs, split/multi-split systems, chillers, and Air Handling Units

What we offer

Van + Fuel Card
33 days Holiday (inc. bank holidays)
Overtime (x1.5 / x2) and Call-out available
Ongoing training and development

New

Contract Management Specialist

Do you have experience in contract management looking to make a significant impa...

Location

Greece , Athens

Salary:

Not provided

Randstad

Expiration Date

December 30, 2025

Requirements

3-5 years of professional experience in contract engineering or contract management, specifically with large-scale EPC projects
Exceptional negotiation, communication, and organizational skills
Proven knowledge of standard contract forms and relevant industry practices
Proficiency with contract management software is a plus
Bachelor’s degree in Engineering (e.g., Civil, Electrical, Mechanical) or related field

Job Responsibility

Contract Management: Oversee the drafting, negotiation, and execution of various contracts, including EPC (Engineering, Procurement, and Construction), O&M (Operation and Maintenance), and PPA (Power Purchase Agreements)
Risk Mitigation: Identify, analyze, and manage contractual risks and liabilities to protect company interests
Compliance: Ensure all contracts adhere to relevant legal, regulatory, and corporate standards
Stakeholder Liaison: Act as the primary point of contact for contractual matters with external partners, suppliers, and internal legal/project teams
Change Control: Manage the contractual change order process, ensuring proper documentation and cost control
Dispute Resolution: Assist in resolving contractual disputes and claims efficiently and favorably

New

Senior Android Developer

Are you an experienced Senior Android Developer ready to make an impact on a glo...

Location

Greece , Athens

Salary:

Not provided

Randstad

Expiration Date

January 05, 2026

Requirements

Understanding of software design principles and architectural patterns
Familiarity with secure coding practices and applying Android UI design principles
Proficiency in Android Studio and Git
Fluency in English
Degree in Information Technology or a related field
4+ years of proven experience in software development with Java and Android

Job Responsibility

Design and develop high-quality, reusable, and efficient Android applications using Java
Collaborate closely with cross-functional teams to translate requirements into innovative technical solutions
Implement secure and robust solutions for payment processing that adhere to the highest industry standards
Identify and resolve software defects while continuously optimizing application performance
Participate in code reviews to promote quality and best practices within the team

Fulltime

Manager Quality Control - Biochemistry Labs

Amgen

Location:
United States, Juncos

Category:
Quality Control

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
December 18, 2025

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Manager Quality Control - Biochemistry Labs

Amgen

Location:United States, Juncos

Category:Quality Control

Contract Type:Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:December 18, 2025

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