Associate
Associate-QualityControl
Neural analysis suggests this role is
optimal for Mid candidates.
“Associate - Quality Control at Associate. Skills: Analytical Method Transfer, Method Validation, Quality Control. Perform method transfers/ validations / method verifications. Interpret and evaluate data for accuracy”
What You'll Achieve.
delivery of safe and effective products; uphold a quality culture; meet targets
Industry & Context.
problem-solving skills; recommending appropriate corrective actions
What They're Looking For.
Must Have
Master’s degree in chemistry/ pharmacy, 2 - 5 years of experience in Analytical Method Transfer / Validation, Qualified in multiple analytical techniques, HPLC, GC, UV‑Vis, FTIR, Karl Fischer, pH meters, Demonstrated technical skills in method validation and testing, Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures, and governmental regulations, Conduct analytical method validation in accordance with ICH Q2 (R1/R2), USP, and EP standards, Conduct test method GAP assessments against USP, EP, BP, and JP requirements for New Product Introduction (NPI), Execute and document analytical method verification and method transfer activities, Knowledge of Good Manufacturing Practices and its application standards, processes, and policies, Excellent organizational skills, ability to multi-task, written and verbal communication skills, Proficiency with unique Quality Control instruments to meet accuracy specifications for sample management, retains management, interpretation, and evaluation
Nice to Have
Experience with laboratory work, analytical HPLC, High Pressure Liquid Chromatography, GC techniques, Proven track record in leading continuous improvement projects, knowledge of lean manufacturing principles, six sigma methodologies, statistical analysis, problem-solving skills, attention to detail, Ability to manage multiple priorities and meet deadlines, Excellent interpersonal skills, ability to communicate effectively with colleagues at all levels, Adaptability, willingness to learn new techniques and procedures
What You'll Do.
Perform method transfers/ validations / method verifications
Interpret and evaluate data for accuracy
Ensure documentation and quality records comply with GMP/GLP
Review and revise Standard Operating Procedures
Conduct analyses on finished products
Contribute to completion of complex projects
Manage time effectively to meet targets
Develop plans for work activities
How You'll Work.
Team & Collaboration
coordination with cross‑functional teams; working under their direction; communicate effectively with colleagues
Communication Scope
written and verbal communication skills; communicate effectively
Process & Methodology
manage time effectively, manage multiple priorities, meet deadlines
Full Job Description
**Associate:** **Use Your Power for Purpose** Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver is of the highest standard. **What You Will Achieve** In this role, you will: * Perform method transfers/ validations / method verifications to the complex analytical techniques * Interpret and evaluate data for accuracy, precision, trends, and potential cGMP impact, recommending appropriate corrective actions. * Ensure all documentation and quality records comply with Good Manufacturing Practices and Good Laboratory Practices and are filed according to existing policies. * Review and revise Standard Operating Procedures, analytical methods, and related documents to keep them current. * Conduct analyses on finished products, raw materials, and components, including data entry, review, and approval in a computerized database. * Contribute to the completion of complex projects, manage time effectively to meet targets, and develop plans for work activities within a team, while exercising judgment with reliance on supervisor and working under their direction. **Here Is What You Need (Minimum Requirements)** * Master’s degree in chemistry/ pharmacy with 2 - 5 years of experience in Analytical Method Transfer / Validation) * Qualified in multiple analytical techniques**(** HPLC, GC, UV‑Vis, FTIR, Karl Fischer, and pH meters) * Demonstrated technical skills in method validation and testing * Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures, and governmental
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