Manufacturing Supervisor (1st shift) - Sanford, NC
Manufacturing Supervisor (1st shift) - Sanford, NC
Posted on :
26-07-2025
Employer Active
1 Vacancy
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Job Description
ATTENTION MILITARY AFFILIATED JOB SEEKERS- Our organization works with partner companies to source qualified talent for their open roles. The following position is available toVeterans Transitioning Military National Guard and Reserve Members Military Spouses Wounded Warriors and their Caregivers. If you have the required skill set education requirements and experience please click the submit button and follow the next steps. Unless specifically stated otherwise this role is On-Site at the location detailed in the job post.
Use Your Power for Purpose
Our breakthroughs would not reach the hands of patients without our dedicated pharmaceutical manufacturing team. We rely on agile members who understand the critical impact of their role in Pfizers mission. Patients need colleagues like you who take pride in their work and continuously strive to improve outcomes. Your efforts ensure that patients and physicians have timely access to the medicines they need.
What You Will Achieve
In this role you will:
Provide supervision to hourly direct reports. Motivate personnel by setting high standards encourage teamwork. Clear unambiguous communication is critical.
Ensure a safe work environment. Ability to identify evaluate and correct potential hazards in the workplace is essential.
Coordinate schedule and participate in daily activities of cGMP production in the manufacturing area to meet supply chain needs.
Must be flexible to work rotating shifts to support 24/7 operation. Ensure that product quality is maintained through all phases of commercial production including operational parameters of manufacturing equipment personnel activities batch record/processing dynamics and integrated utilities to identify and resolve quality risk to commercial manufacturing. General knowledge of scientific principles production equipment and related procedures.
Aid in investigations. Responsible for the adherence to established policies procedures and practices. Participate in inspections and cGMP and Quality decisions effecting short term production
Primary contact for all personnel issues occurring within the department. Responsible for development plans and personnel reviews. Make initial decisions encompassing personnel issues disciplinary actions career advancement educational assistance Emergency situations including injured employees facility issues and inclement weather.
Review completed batch records. Develop training material update curricula close training gaps support the training of new supervisors.
Advise management of non-conformance issues and opportunities for continuous improvement
Provide input on primary decisions on cGMP related documents developed or revised.
Articulate challenges and solutions to technical and non-technical peers and to department management.
Provide technical guidance and act as a departmental liaison with primary support groups.
Short range planning includes scheduling daily and weekly operations and staff. Longer range planning concerns facilities shutdowns and preventive maintenance.
Use Your Power for Purpose
Our breakthroughs would not reach the hands of patients without our dedicated pharmaceutical manufacturing team. We rely on agile members who understand the critical impact of their role in Pfizers mission. Patients need colleagues like you who take pride in their work and continuously strive to improve outcomes. Your efforts ensure that patients and physicians have timely access to the medicines they need.
What You Will Achieve
In this role you will:
Provide supervision to hourly direct reports. Motivate personnel by setting high standards encourage teamwork. Clear unambiguous communication is critical.
Ensure a safe work environment. Ability to identify evaluate and correct potential hazards in the workplace is essential.
Coordinate schedule and participate in daily activities of cGMP production in the manufacturing area to meet supply chain needs.
Must be flexible to work rotating shifts to support 24/7 operation. Ensure that product quality is maintained through all phases of commercial production including operational parameters of manufacturing equipment personnel activities batch record/processing dynamics and integrated utilities to identify and resolve quality risk to commercial manufacturing. General knowledge of scientific principles production equipment and related procedures.
Aid in investigations. Responsible for the adherence to established policies procedures and practices. Participate in inspections and cGMP and Quality decisions effecting short term production
Primary contact for all personnel issues occurring within the department. Responsible for development plans and personnel reviews. Make initial decisions encompassing personnel issues disciplinary actions career advancement educational assistance Emergency situations including injured employees facility issues and inclement weather.
Review completed batch records. Develop training material update curricula close training gaps support the training of new supervisors.
Advise management of non-conformance issues and opportunities for continuous improvement
Provide input on primary decisions on cGMP related documents developed or revised.
Articulate challenges and solutions to technical and non-technical peers and to department management.
Provide technical guidance and act as a departmental liaison with primary support groups.
Short range planning includes scheduling daily and weekly operations and staff. Longer range planning concerns facilities shutdowns and preventive maintenance.
Additional Qualifications/Responsibilities
Here Is What You Need (Minimum Requirements)
Bachelors Degree in Engineering Business or Science with a minimum of 2 years of experience and 1 years of demonstrated leadership capability in a pharmaceutical and/or manufacturing environment OR Masters degree with some experience and 1 years of demonstrated leadership capability in a pharmaceutical and/or manufacturing environment OR Associates Degree with a minimum of 6 years of experience and 3 years demonstrated leadership capability in a pharmaceutical and/or manufacturing environment OR High School Diploma with a minimum 8 years of experience and 5 years demonstrated leadership capability in a pharmaceutical and/or manufacturing environment
Working knowledge of vaccine or biotechnology product manufacturing in a cGMP environment. Including a working knowledge of fermentation purification centrifugation homogenization Ultrafiltration and Diafiltration (UF/DF) aseptic techniques and other filtration processes.
Physical / Mental requirements
Requires the moving of heavy equipment and the ability to lift 40 pounds.
Strong problem-solving skills in a structured environment
Non-Standard work schedule travel or environment requirements
Supports a 24/7 facility. M-F 1st Shift 6:00AM-2:30PM.
Ability to support operations and training in other shifts when needed.
Ability to work weekends when needed (non-standard)
Other job details
Employee Referral Bonus eligible
Work Location Assignment: On Premise
The annual base salary for this position ranges from $80300.00 to $133900.00. In addition this position is eligible for participation in Pfizers Global Performance Plan with a bonus target of 10.0% of the base salary. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of lifes moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution paid vacation holiday and personal days paid caregiver/parental and medical leave and health benefits to include medical prescription drug dental and vision coverage. Learn more at Pfizer Candidate Site U.S. Benefits (). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa FL or any location outside of the United States.
Required Experience:
Manager
Employment Type
Part-Time
Key Skills
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