Job Description
Assist with initial and subsequent validation of a new area, including manufacturing equipment and processes. Collaborate with cross-functional teams, including Quality Assurance, Quality Control, and Maintenance, to troubleshoot issues and resolve deviations. Participate in aseptic process simulations, media fills, and equipment qualifications. Participate in in-process inspections and quality control checks to verify the integrity of product quality. Complete applicable logbook, form, and batch record documentation as required while adhering to strict cGMP and Good Documentation Practices. Contribute to continuous improvement initiatives by identifying opportunities to enhance processes, reduce waste, and increase efficiency. Complete initial aseptic gowning and process qualification and maintain qualification to work within Grade A and Grade B cleaning environment. Comply with policies, guidelines, and regulatory requirements of the Quality System and applicable current Good Manufacturing Practices (cGMPs). Other duties as required and assigned by management.
ResponsibilitiesAssist with initial and subsequent validation of new manufacturing areas, equipment, and processes.Collaborate with Quality Assurance, Quality Control, and Maintenance teams to troubleshoot issues and resolve deviations.Participate in aseptic process simulations, media fills, and equipment qualifications.Conduct in-process inspections and quality control checks to ensure product quality.Complete logbook, form, and batch record documentation in accordance with cGMP and Good Documentation Practices.Identify opportunities for process improvement to enhance efficiency and reduce waste.Complete and maintain aseptic gowning and process qualifications for Grade A and Grade B cleaning environments.Adhere to Quality System policies, guidelines, and regulatory requirements, including cGMPs.Perform other duties as assigned by management.Essential SkillsMinimum 1 year of experience in the pharmaceutical, biopharma, or biotech industry, particularly in aseptic clean room environments.Knowledge of aseptic gowning techniques, cleanroom protocols, and cGMP.Ability to read and comprehend work instructions and standard operating procedures.Capability to understand equipment alarms and escalate issues as necessary.Exceptional attention to detail, accuracy, and documentation skills.Ability to work in a controlled aseptic environment, following gowning and hygiene protocols.Good communication skills and the ability to work collaboratively in a team-oriented environment.Additional Skills & QualificationsHigh school diploma or equivalent; additional technical or vocational education is a plus.Flexibility to work in shifts, including evenings, nights, weekends, and holidays, as required by production schedules.Work Environment
The position involves working in Grade A and B clean rooms. Aseptic gowning is essential. There are two openings: one for the first shift and one for the second shift. Employees must adhere to strict gowning and hygiene protocols. The work environment requires flexibility to work various shifts, including evenings, nights, weekends, and holidays as needed.
Pay and Benefits
The pay range for this position is $28.00 - $28.00/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 fully onsite position in Parsippany,NJ.
Application Deadline
This position is anticipated to close on Mar 7, 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 & InclusionAt 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 peopleThe 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 for other accommodation options.