Job Description
We are seeking an entry-level Biologic Operator I to join our team, working Wednesday through Saturday from 1pm to 11:30pm. This role involves working in aseptic high-level silent environments, performing repetitive tasks such as syringe inspections, and operating in conditions with low light and cold temperatures ranging from 15 to 25 degrees, with occasional exposure to temperatures as low as 2 to 8 degrees.
ResponsibilitiesConduct production of highly expensive and sensitive biological parenteral products.Perform cleaning and preparation of equipment, solution formulation, process testing, filtering, and transfer of solutions.Provide support in aseptic filling of small volume syringes using Restricted Access Barrier Systems (RABS) and inspect the filled product in its final packaging.Operate different equipment such as parts washers, autoclaves, CIP and SIP systems, formulation tanks, filter integrity testing machines, and magnetic stirrers.Make inventory of materials and parts necessary for manufacturing and perform process tests as required.Monitor alarm systems and assemble equipment for cleaning and sterilization procedures.Comply with Good Manufacturing Practices (GMP) and standard procedures (SOPs).Inform the supervisor of any events occurring during the work shift.Work aseptically in the formulation of biological parenteral products and perform process samples such as pH, density, and osmolality.Inspect equipment to ensure operation within established parameters.Carry out cleaning operations, pressure testing, sterilization of equipment, integrity of filters and RABS gloves, filtration of solutions, aseptic filling, and product inspection.Monitor processes through computerized systems and visual inspection, recognizing deviations to alert and take corrective actions.Receive and verify materials for final product manufacturing.Participate and assist in qualification and validation activities within the SVP area.Maintain detailed records of operations during shifts, including batch records and logbooks, and perform inventory transactions.Handle and dispose of hazardous and non-hazardous materials according to established procedures.Attend and complete training on industrial hygiene, occupational safety, and GMPs.Use required personal protective equipment (PPE) and notify supervisors of incidents or unsafe conditions.Operate efficiently to achieve optimal product performance.Complete production documentation accurately and on time, following good documentation practices.Audit batch records and logbooks of production as required.Maintain clean facilities to ensure aseptic conditions.Diagnose and resolve complex equipment and process issues using systems such as Human Machine Interface (HMI) and Process Logics Controls (PLC).Assist in other SVP areas as necessary.Provide assistance in managing and disposing of domestic, biomedical, and hazardous waste, ensuring compliance with regulations.Essential SkillsProduction experienceInspection skillsAseptic technique proficiencyKnowledge of Good Manufacturing Practices (GMP)Biology degree1-2 years of relevant work experienceAdditional Skills & QualificationsUnderstanding and basic knowledge of automated systemsAbility to sit in the same position for extended periodsAbility to work in cold environmentsStrong attention to detail and documentation skillsWork Environment
The role operates Wednesday through Saturday from 1pm to 11:30pm. You will work in aseptic high-level silent environments, performing repetitive tasks such as syringe inspections. The work involves low light conditions and cold temperatures ranging from 15 to 25 degrees, with occasional exposure to temperatures as low as 2 to 8 degrees. Personal protective equipment (PPE) is required, and adherence to safety protocols is mandatory.
Pay and Benefits
The pay range for this position is $20.00 - $22.00/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 Branchburg,NJ.
Application Deadline
This position is anticipated to close on Jun 23, 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.
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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.