Associate Manager
AssociateManager-QualityControl
Neural analysis suggests this role is
optimal for Mid candidates.
“Associate Manager - Quality Control at Associate Manager. Skills: Analytical Method Transfer, Method Validation, Quality Control, cGMP. Perform method transfers/ validations/ verifications. Interpret and evaluate data”
What You'll Achieve.
Ensure delivery of safe and effective products; Uphold a quality culture; Meet targets; Ensure effective process control; Timely implementation and closure of CAPA actions
Industry & Context.
problem-solving skills
What They're Looking For.
Must Have
Master’s degree in chemistry/ pharmacy, 5-7 years of experience in Analytical Method Transfer / Validation, Qualified in multiple analytical techniques, HPLC-with Empower, GC, IC, ICP-MS, Potentiometry, 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, Execute and document analytical method verification and method transfer activities, Demonstrate knowledge of ICH Q9 (Quality Risk Management), Perform identification, assay, purity, and related analytical tests using validated methods, Monitor critical process parameters (CPPs) and critical quality attributes (CQAs), Support process validation and troubleshooting, Manage working standards in compliance with established procedures, Handle change control activities, Knowledge of Good Manufacturing Practices, Excellent organizational skills, Ability to multi-task, written and verbal communication skills, Proficiency with unique Quality Control instruments
Nice to Have
Experience with laboratory work, analytical HPLC, GC, IC, ICP-MS 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, 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/ verifications
Interpret and evaluate data
Ensure documentation compliance
Review and revise SOPs
Conduct analyses on products
Contribute to complex projects
Manage time effectively
Develop plans for work activities
How You'll Work.
Team & Collaboration
Coordination with cross-functional teams; Communicate analytical results promptly to Production and QA; Communicate effectively with colleagues at all levels
Communication Scope
written and verbal communication skills; Ability to communicate effectively
Process & Methodology
Manage time effectively, Develop plans for work activities, Manage multiple priorities, Meet deadlines, Lead continuous improvement projects
Full Job Description
**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 5-7 years of experience in Analytical Method Transfer / Validation) * Qualified in multiple analytical techniques**(** HPLC-with Empower, GC, IC, ICP-MS, Potentiometry, 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 proced
Applying for this Associate Manager - Quality Control role?
Most applicants get filtered before a human reads their resume. See if yours makes the cut.
How to Apply on Workday
- Workday has a multi-step form — save your progress after every section.
- "Apply With LinkedIn" can fail or lose data; manual entry is more reliable.
- Watch for the "Submit for Review" final step — hitting "Save" alone does not submit.
- Job requisition numbers are useful when following up with HR by email.
ANONYMOUS · UNFILTERED
What do employees actually say about Associate Manager?
Real rants from real employees. Read before you apply.