Job Description
Peoplelink Staffing, in partnership with a major pharmaceutical company, is actively searching for exceptional candidates to fill the position of Pharmaceutical Packaging Operator. If you have a strong work history in production, GMP factories, or relevant fields, and are ready for a multi-step interview process, we encourage you to apply.
Pharmaceutical Packaging Operator Benefits:
Onsite gym
Restaurant quality canteen
Great career growth opportunities with a company that promotes from within
Climate controlled environment and immaculate cleanliness
Competitive starting pay rate of $20.86/hr
Department: Packaging
Title: Packaging Operator
Function: Operations
Shift: 1st/2nd shift bi weekly rotation, straight 3rd shift available.
1st - 7am-330pm (NOT AVAILABLE)
2nd- 3pm-1130pm (NOT AVAILABLE)
3rd- 11pm-730am (Sunday night and going until Friday morning, candidate would have to be 3rd shift preference but would train on the rotation until they went to 3rd)
The Packing Operator is responsible for producing packaged pharmaceutical products in a safe and efficient manner, complying with cGMP’s, SOPs, and site safety procedures.
We have several shift positions available.
Responsibilities:
o Operate packing equipment (tablet fillers, thermoforms, labelers, case packers, etc.) in a safe and efficient manner.
o Must understand and comply with cGMP’s, SOPs and site safety procedures.
o Verify correctness of product and components for the NDC packaged.
o Supply equipment with components and product. Lifting requirements may be up to 50 lbs.
o Perform detection system challenges on applicable equipment.
o Perform basic maintenance, changeover, set up, and troubleshooting of packaging equipment.
o Clean, purge, and inspect packaging equipment.
o Accountable for accurately documenting, packing, and cleaning activities in logbooks and electronic systems.
o Perform quality attribute inspections and in-process testing (torques, induction seal integrity, leak tests, appearance, etc.)
o Rework packages according to SOPs or Rework Packaging Order to correct deviations.
o Attend regular SHE and GMP meetings.
o Share knowledge with co-workers for training purposes.
o Work effectively in teams to meet monthly demand requirements.
o Identify areas for continuous improvement and efficiency improvements, and implement fixes for these ideas.
o Accountable for Line performance (OEE) and able to report hourly status of line to affected personnel to ensure timely resolution to issues. (i.e. Facilitators, Engineers).
o Must be able to work off shifts, weekends, alternative schedules, and rotate between shifts when production demands require.
o Must be flexible to change.
o Ability to perform duties with minimum supervision.
o Conduct activities and interactions consistent with Company values and in compliance with the Code of Ethics and supporting Policies and Standards relevant to your role.
o Complete all required training on the Code of Ethics and supporting Policies and Standards on time. Report potential issues of non-compliance.
o Ensures compliance with Corporate Policies and Directives, site Standard Operating Procedures, site policies, work instructions, regulatory requirements, and industry best practice (cGMPs, GAMP, ITIL, PMI).
o Maintains a safe work environment and performs work in accordance with site, Safety, Health, and Environment (SHE) policies and procedures.
o Immediately report potential unsafe conditions to management.
o Supports internal, external, and regulatory inspections including FDA, EMEA, and third-party inspections.
o Participates in the investigation and resolution of product quality problems.
Qualifications:
Education:
o High School Diploma / GED required
Required:
o Excellent verbal, written, and interpersonal communication skills.
o Basic mechanical aptitude.
o Basic computer skills.
Preferred:
o Minimum of one (1) year experience in production environment, preferably pharmaceuticals.
o Experience in pharmaceutical production environment.
o Knowledge of cGMPs.