Pharmaceutical Attendant
About the role
Take responsibility for individual contributions to achieve team deliverables, working effectively as a team member and coordinating with others.
Manage personal time and professional development, being accountable for results.
Follow standard procedures to complete tasks of varying scope, sequence, and complexity within the agreed timeframe.
Identify and solve moderately routine problems.
Complete assignments with moderate supervision using established procedures, referring deviations from standard procedures to the supervisor.
Ensure work is reviewed for accuracy, quality, and adherence to standards.
Prepare and operate various components, materials, equipment, and machines in your assigned area, ensuring adequate inventory of parts and materials before starting a production run.
Adhere strictly to all plant safety and current Good Manufacturing Practices (cGMP) regulations.
Perform in-process quality inspections, and seek to implement process and safety improvements.
Responsibilities
- Take responsibility for individual contributions to achieve team deliverables, working effectively as a team member and coordinating with others.
- Manage personal time and professional development, being accountable for results.
- Follow standard procedures to complete tasks of varying scope, sequence, and complexity within the agreed timeframe.
- Identify and solve moderately routine problems.
- Complete assignments with moderate supervision using established procedures, referring deviations from standard procedures to the supervisor.
- Ensure work is reviewed for accuracy, quality, and adherence to standards.
- Prepare and operate various components, materials, equipment, and machines in your assigned area, ensuring adequate inventory of parts and materials before starting a production run.
- Adhere strictly to all plant safety and current Good Manufacturing Practices (cGMP) regulations.
- Perform in-process quality inspections, and seek to implement process and safety improvements.
Requirements
- High School Diploma or GED with 1+ year of relevant experience
- Strong analytical and problem-solving skills
- Excellent problem-solving and decision-making skills
- Excellent communication and interpersonal skills
- Ability to work independently and as part of a team
- Detail-oriented with strong organizational skills
Qualifications
- Previous experience in cGMPs (current Good Manufacturing Practices) environment
- Proficiency in using manufacturing software and tools
- Ability to adapt to changing priorities and work in a fast-paced environment
- Demonstrated leadership skills and ability to mentor team members
- Familiarity and basic understanding of common AI tools and a curiosity for learning how they can be used to enhance productivity
SkillsKnowledge of pharmaceutical manufacturing and regulatory compliance
Benefits
- Comprehensive and generous benefits and programs
- Includes 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
- Health benefits to include medical, prescription drug, dental and vision coverage
Pay
The salary for this position ranges from $18.99 to $31.65 per hour. In addition, this position offers eligibility for overtime, weekend, holiday and other pay premiums depending on the work schedule and the Company's policies.
Schedule
24x7 operations with a rotating 12-hour night shift schedule. Will work alternating weekends and holidays based on A/B shift schedule.
Location
On Premise
Other Job Details
- Last Date to Apply for Job (Internal Candidates): July 22nd, 2026
- Last Date to Apply for Job (External Candidates): July 29th, 2026