Manufacturing Supervisor

#MFG175-N, #MFG178-N, #MFG-199, #MFG-206-NWe currently have several openings for Manufacturing Supervisors. Two positions are in our Purification department on the rotating night shift, 7pm - 7am.  We also have two openings in our Fermentation department; one on the rotating day shift, 7 am - 7 pm and one on the rotating night shift. There is a 20% pay differential for the night shift.

Position ResponsibilitiesDaily review of production schedule and priorities to determine shift assignments and critical actions. Ensure all materials and batch records to support shift requirements and any off shift needs for the day. Oversee all tasks on the floor as they are carried out and provide assistance and troubleshooting where needed. Provide 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. Monitor operator training files and work with compliance specialist to keep files up to date. Communicate end of shift status to the next shift supervisor and to the unit manager as required for smooth hand off on a daily basis. Use the day book approach to manage the days goals and responsibilities in line with the priorities. Review, on a shift wide basis, the batch records for error and deviations, signing off responsibility to the next supervisor after this review. Ensure that all log books and sanitation tasks have been completed after each shift. Closeout logbook and return to QA at completion or changeover. Work with compliance specialist and process technologist to resolve deviations. Work with technology transfer associates to incorporate new cell lines and processes in the plant. Oversee the generation and review of Batch records and SOP's. Provide continued motivational and team building atmosphere. Help management to provide a path for operators and school them to advancement. Responsible to help forecast and meet indirect materials budgets and overtime budgets. Work interdepartmentally to see that work orders, dispensing, preventative maintenance, QC, and documentation issues are resolved and enhance communications at all levels.

Position RequirementsKnowledge of cell culture or purification of biological drugs is required. Management, leadership, supervision, time management, detail oriented, written and oral communication skills, computer proficiency, scheduling experience.
5+ years of biotech or pharmaceutical manufacturing industry experience
1+ years of supervisory experience
1-2 years of Manpower planning/scheduling


Are you interested?Send resume and cover letter to resumes@lonza.com Please apply for only one position per submission. Only resumes with a valid job title and reference code will be accepted.

About UsLonza Biologics is the world's leading contract manufacturer of monoclonal antibodies and recombinant proteins derived from mammalian cell culture. We provide clients with a comprehensive array of services ranging from cell line construction and development through cell banking to large-scale cGMP manufacture and purification. We are located in the picturesque seacoast community of Portsmouth, NH (50 miles north of Boston).

A great place to work offering a competitive income and an excellent benefits program that includes: 100% matching 401K program, 120 hours/year vacation, bonus scheme and tuition reimbursement (books and fees included) for 2 courses each semester.

Lonza Biologics is an Equal Opportunity Employer.