Lead Formulation Technician (12hr days or 12hr nights, 2-2-3 rotation)

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profile Job Location:

Greenville, NC - USA

profile Monthly Salary: Not Disclosed
Posted on: Yesterday
Vacancies: 1 Vacancy

Job Summary

Work Schedule

12 hr shift/nights

Environmental Conditions

Able to lift 40 lbs. without assistance Adherence to all Good Manufacturing Practices (GMP) Safety Standards Cleanroom: no hair products jewelry makeup nail polish perfume exposed piercings facial hair etc... allowed Loud Noises (Equipment/Machinery) Some degree of PPE (Personal Protective Equipment) required (safety glasses gowning gloves lab coat ear plugs etc.) Standing for full shift

Job Description

As part of the Thermo Fisher Scientific team youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the worlds toughest challenges like protecting the environment making sure our food is safe or helping find cures for cancer.

Location/Division Specific Information:
Greenville NC/DPD

How Will You Make an Impact:

As aTeam Leader in Formulation Manufacturing you will lead a skilled team of manufacturing technicians dedicated to producing sterile pharmaceutical products that meet the highest standards of quality and compliance. Youll coordinate daily operations mentor and develop team members and help ensure that every batch meets safety and quality expectations.


A Day in the Life:

  • Own the terminal sterilization process and review paperwork to ensure completion and compliance.

  • Ensure operations are performed in a safe and responsible manner striving to create an injury-free and incident-free workplace.

  • Ensure pharmaceutical products in manufacturing are in accordance to Standard Operating Procedures (SOPs) and Current Good Manufacturing Practices (cGMPs) and other batch related activities.

  • Verify and document production activities in batch records logbooks etc.

  • Assist in troubleshooting operational and production problems in order to identify appropriate corrective actions.

  • Perform the disassembly assembly cleaning and operation of area manufacturing equipment. Prepare equipment and components for operations.

  • Assist in the commissioning of new equipment and production areas. Assist in initial and subsequent validation of equipment and processes.

  • Maintain/clean classified environments/areas.

  • Communicate and work to resolve any production quality or safety issues.

  • Comply with all job-related safety cGMP and other department procedural requirements.

  • Participate in the On the Job (OJT) training program area safety initiatives and area lean manufacturing initiatives.

  • Train new employees.

  • Perform other duties as assigned.


Education:

  • High School Diploma or equivalent required


Experience:

  • Required: Minimum of three (3) years of experience in pharmaceutical biopharmaceutical or sterile manufacturing four (4) years preferred.

  • Equivalent combinations of education training and relevant work experience may be considered.

  • Hands-on experience in aseptic or sterile product formulation and using SAP or other manufacturing systems strongly preferred.


Knowledge Skills Abilities:

  • General mechanical electrical/electronic pneumatic and hydraulic knowledge of pharmaceutical industry equipment.

  • Effective verbal and written communication skills.

  • Basic computer skills.

  • Strong interpersonal skills.

  • Ability to work independently.

  • Flexibility with departmental work schedules including overtime and all shift operations.

  • Ability to achieve and maintain qualifications to work in a cleanroom environment.

  • Ability to drive a fork lift and other mobile equipment to locate product and equipment as needed.



Physical Requirements / Work Environment
Position requires ordinary ambulatory skills and physical coordination sufficient to move about office locations; ability to stand walk stoop kneel crouch periodically for prolonged periods of time; manipulation (lift carry move) of medium weights of 25-50 pounds; occasionally pushing and pulling 50-100 pounds; arm hand and finger dexterity including ability to grasp and type for prolonged periods of time; visual acuity to use a keyboard computer monitor operate equipment and read materials for prolonged periods of time; ability to sit reach with hands and arms talk and hear for prolonged periods of time. Ability to climb stairs and ladders. Full range of motion in upper and lower extremities.

What We Offer:

Compensation
Competitive Pay
Performance Related Bonus where eligible
Annual merit performance-based increase

Excellent Benefits
Medical benefits
Paid Time Off/Annual Leave
Employee Referral Bonus
Career Advancement Opportunities


Required Experience:

IC

Work Schedule12 hr shift/nightsEnvironmental ConditionsAble to lift 40 lbs. without assistance Adherence to all Good Manufacturing Practices (GMP) Safety Standards Cleanroom: no hair products jewelry makeup nail polish perfume exposed piercings facial hair etc... allowed Loud Noises (Equipment/Machi...
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