Description Provide quality oversight for drug product process technology transfers, including development Provide quality oversight for drug product process qualification/validation protocol, exception, and report reviews Provide quality validation oversight at contract manufacturing organizations (CMOs), including continued process verification (CPV), product quality reviews (PQR), supporting investigations and deviations as needed Support process validation and tech transfer across all departments Understood risk management principles Skills Validation protocols, Validation, CMO, tech transfer, Process improvement, FDA, ICH, GMP, Iq oq, Pq Top Skills Details Validation protocols,Validation,CMO,tech transfer,Process improvement Additional Skills & Qualifications 8-12 years of relevant experience and bachelor’s degree in science or related field. Biopharmaceutical or Pharmaceutical experience preferred Direct experience in process qualification and validation using FDA and ICH guidance required. Direct experience working with a CMO and drug product manufacturing preferred Knowledge of biologics/gene therapy processes desirable Must have in-depth understanding and application of GMP and validation principles, concepts, practices and standards in the US and internationally Experience Level Expert Level Pay and Benefits The pay range for this position is $63.00 - $82.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision• Critical Illness, Accident, and Hospital• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available• Life Insurance (Voluntary Life & AD&D for the employee and dependents)• Short and long-term disability• Health Spending Account (HSA)• Transportation benefits• Employee Assistance Program• Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a hybrid position in Andover,MA. Application Deadline This position is anticipated to close on Feb 14, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: + Hiring diverse talent + Maintaining an inclusive environment through persistent self-reflection + Building a culture of care, engagement, and recognition with clear outcomes + Ensuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.