GMP Clinical Packaging Specialist

Pfizer Inc.; Groton (CT); On-site; USD 37,000 - 62,000; Full time

Job summary

Pfizer Inc. in Groton, CT is seeking an experienced packaging operator to perform primary and secondary packaging for clinical materials. You will count, fill, label, and package solid-dose forms, while maintaining equipment and recording activities in GMP-compliant documentation.

The role emphasizes collaboration, adherence to SOPs, and safe handling of materials, with daily use of EMD365 and a focus on meeting team targets. This is a first-shift position with strong benefits.

Qualifications

• High School Diploma or equivalent.
• 4+ years of relevant experience.
• Excellent documentation skills and attention to detail.
• Computer literacy in Microsoft Word.
• Strong computer, scientific, and organizational skills.
• Excellent communication (oral and written) and attention to detail.
• Ability to work as part of a team, self-motivated, adaptable, and positive.
• Ability to learn new techniques and follow instructions.

Responsibilities

• Perform primary and secondary packaging operations in a GMP environment following batch records.
• Complete GMP documentation to record equipment used and packaging activities.
• Adhere to SOPs, cGMPs, and safety requirements for handling materials.
• Use EMD365 to scan material and perform packaging tasks.
• Maintain packaging rooms and equipment through routine maintenance and cleaning.
• Support production schedules and timelines; assist in resolving equipment issues.

Skills

Documentation skills

attention to detail

MS Word

teamwork

learning new techniques

communication skills

adaptability

Education

High School Diploma or equivalent

4+ years of relevant experience

Tools

EMD365

GMP packaging equipment

Job description

Pfizer Inc. in Groton, CT is seeking an experienced packaging operator to perform primary and secondary packaging for clinical materials. You will count, fill, label, and package solid-dose forms, while maintaining equipment and recording activities in GMP-compliant documentation.

The role emphasizes collaboration, adherence to SOPs, and safe handling of materials, with daily use of EMD365 and a focus on meeting team targets. This is a first-shift position with strong benefits.