Associate
Healthcare
Associate-QualityControl
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Associate - Quality Control at Associate. Skills: Quality Control, Analytical Methods, Method Validation. Perform method transfers/validations/verifications. Interpret and evaluate data for accuracy”
What You'll Achieve.
Deliver safe and effective products; Uphold quality culture; Meet targets
Industry & Context.
Problem-solving skills; Recommend corrective actions
What They're Looking For.
Must Have
Master’s degree in chemistry/pharmacy, 2-5 years experience, Analytical Method Transfer / Validation experience, Qualified in multiple analytical techniques, Demonstrated technical skills in method validation, Ability to read and understand applicable compendial methods, 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, Knowledge of Good Manufacturing Practices, Excellent organizational skills, Ability to multi-task, Proficiency with unique Quality Control instruments
Nice to Have
Experience with laboratory work, Experience using analytical HPLC, Experience using GC techniques, Proven track record in leading continuous improvement projects, Knowledge of lean manufacturing principles, Knowledge of six sigma methodologies, Knowledge of statistical analysis, Ability to manage multiple priorities, Ability to meet deadlines, Adaptability and willingness to learn new techniques
What You'll Do.
Perform method transfers/validations/verifications
Interpret and evaluate data for accuracy
Recommend appropriate corrective actions
Ensure documentation complies with GMP/GLP
File quality records according to policies
Review and revise Standard Operating Procedures
Review and revise analytical methods
Conduct analyses on finished products
Conduct analyses on raw materials
Conduct analyses on components
Contribute to completion of complex projects
Manage time effectively to meet targets
Develop plans for work activities
Exercise judgment with reliance on supervisor
Work under supervisor's direction
How You'll Work.
Team & Collaboration
Coordination with cross-functional teams; Work activities within a team
Communication Scope
Written communication; Verbal communication; Interpersonal skills
Process & Methodology
Manage time effectively, Develop plans for work activities
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 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 regulations * C
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