Supervisor Manufacturing - Onsite
Supervisor Manufacturing - Onsite
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Not Disclosed
Salary Not Disclosed
1 Vacancy
Job Description
Responsible for the daily supervision and training of operating personnel in the production of clinical or commercial products. Works in concert with other supervisors. Responsible for the accurate and timely completion of production related cGMP documentation. Facilitates the transfer planning implementation and maintenance of manufacturing processes and procedures. Ensures the effective use of material equipment and personnel in producing quality products.
Responsibilities:
- Develops weekly goals and schedules and set priorities for staff. Reviews weekly production schedule and priorities to determine unit assignments and critical actions.
- Reviews all materials and batch records required to support shift and any off shift needs for the day.
- Provides on the floor training to support formalized technical and GMP training. Check that operator training files match and support the processes they are required to carry out.
- Monitors operator training files and work with compliance specialist to keep files up to date.
- Works with QA and Subject Matter Expert (Tech Ops or Process Sciences) to resolve exceptions. Reviews new Batch records and SOPs.
- Works with technology transfer team to incorporate new processes in the plant.
Works interdepartmentally to see that work orders dispensing preventative maintenance QC and documentation issues are resolved and enhances communications at all levels. - Ensures that direct materials budgets and overtime budgets are met.
- Provides supervision primarily to skilled nonexempt and junior level exempt employees. Acts as advisor to unit or subunit becomes actively involved as required. Acts as mentor for less senior personnel.
Evaluates staff performance. - Ensures compliance with all applicable local state and federal regulatory requirements which include but are not limited to: OSHAs Process Safety Management (PSM) standard (29 CFR 1910.119) and EPAs Risk Management Planning (RMP) rule (40 CFR 68) Mechanical Integrity programs PCI DOT EPA etc.
- Creates a safety culture by setting direction to reduce or eliminate operationsrelated injuries or accidents damage/loss of product or equipment and unnecessary costs by ensuring that all equipment and facilities are maintained consistent with the safety security hygiene and standards set by AbbVie.
Qualifications :
- Requires a Bachelors degree or equivalent; Eight plus years experience in all aspects of manufacturing/ production processes
- Computer proficiency and scheduling experience required; good writing skills.
- Working knowledge of safety quality systems and cGMPs is required
- Familiarity with industrial automation (e.g. distributed control and PLCbased systems
- Familiarity with equipment and facilities validation
Additional Information :
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location and we may ultimately pay more or less than the posted range. This range may be modified in the future.
We offer a comprehensive package of benefits including paid time off (vacation holidays sick) medical/dental/vision insurance and 401(k) to eligible employees.
This job is eligible to participate in our shortterm incentive programs.
Note: No amount of pay is considered to be wages or compensation until such amount is earned vested and determinable. The amount and availability of any bonus commission incentive benefits or any other form of compensation and benefits that are allocable to a particular employee remains in the Companys sole and absolute discretion unless and until paid and may be modified at the Companys sole and absolute discretion consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives serving our community and embracing diversity and inclusion. It is AbbVies policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race color religion national origin age sex (including pregnancy) physical or mental disability medical condition genetic information gender identity or expression sexual orientation marital status status as a protected veteran or any other legally protected group status.
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US & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:
Remote Work :
No
Employment Type :
Fulltime
Employment Type
Full-time
