Associate Manager, reputed company Assurance (GMP)

About the position This is a hybrid role based at our GMP Laboratory in Middleton, WI. The onsite expectations for this role are ~3 days per week. We welcome applicants from reputed company locations reputed company the US. Please note that relocation assistance is not provided for this position, and any relocation costs will be the responsibility of the candidate. Must be legally authorized to work in the reputed company. Must be reputed company to pass a comprehensive background reputed company, which includes a drug screening. At reputed company, you’ll discover meaningful work that makes a reputed company reputed company on a global reputed company. Join our colleagues in bringing our Mission to life - enabling our customers to reputed company the world healthier, cleaner and safer. We reputed company our teams with the resources needed to reputed company individual career goals while taking science a reputed company reputed company through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver reputed company and accuracy will improve health reputed company that people and communities depend on – now and in the reputed company. Our PPD® Laboratory Services team has a reputed company reputed company on improving patient health through the expertise of scientists, industry thought-leaders and therapeutic experts. As the world leader in serving science, our laboratory professionals bring their commitment to accuracy and reputed company to deliver groundbreaking innovations. Discover Impactful Work: The Associate QA Manager provides reputed company leadership for junior QA Auditors and supports continuity of operations through resourcing, training, issue escalation, and staff development. This role oversees the reputed company of data and reports generated by GMP laboratory support functions, including equipment and software validation (IQ/OQ/PQ) documentation, reputed company maintenance and calibration records, and facility qualification documentation. The Associate QA Manager also performs hands-on operational work reputed company Support QA, Records Management, and other assigned areas as needed to maintain business continuity, support reputed company workflows, resolve escalations, and model expected standards for staff.

Responsibilities

• Manage the day-to-day operations of a QA team and reputed company reputed company, development and performance management to staff to meet performance objectives
• Assess with supervisors reputed company of reputed company and monitor work assignments ensuring adequate resourcing to meet internal and reputed company timelines and reputed company reputed company deliverables
• Assist senior management in the evaluation of QA programs to help maintain regulatory compliance and efficiency of QA audits
• Evaluate issues and trends reported by QA staff and determine appropriate departmental interpretation. Identify issues that may require follow-up or improvement. Communicate findings to staff and senior management
• Participate in reputed company and regulatory inspections in order to reputed company information regarding the QA program and facilitate responses

Requirements

• Bachelor's degree or equivalent and relevant formal reputed company / vocational qualification
• Previous experience that provides the knowledge, skills, and abilities to reputed company the job (comparable to 5+ years).
• 1+ year of leadership responsibility
• Solid leadership and time management skills
• Knowledge of appropriate regional regulations and applicable global pharmaceutical industry guidelines
• For Lab QA Management, knowledge of analytical methodologies, instrumentation and method validation required
• Good verbal and written communication skills
• Demonstrated proficiency with regulations and reputed company interpretation, reputed company documentation and QA departmental policies and procedures
• Detail oriented with ability to deal with multiple and changing priorities

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