Pharmaceutical Production Technician

Spherion; Indianapolis (IN); On-site; USD 37,195 - 41,328; Full time

Benefits offered by this job

Medical insurance

401(k) plan

Short-term disability

Job summary

JobRx, Inc. is hiring a Pharma Production Technician in Indianapolis, IN. The role includes responsibilities in a GMP environment, focusing on aseptic filling and equipment management. Candidates should have at least 5 years of experience in a regulated manufacturing setting.

Position offers competitive pay between $27 to $30 per hour and includes benefits such as medical, dental, and a 401(k) after eligibility. Interested candidates should contact via email at [e-mail].

Qualifications

• Minimum of five years of experience in GMP regulated facility.
• Proficient in reading GMP documentation.
• Leadership experience in training others.

Responsibilities

• Certify for entry into the GMP cleanroom.
• Execute aseptic fill processes.
• Provide training for new team members.
• Ensure calibration of equipment and sanitization.

Skills

Bulk formulation knowledge

Equipment cleaning and preparation

Microsoft Office skills

Education

B.S. degree in chemistry, biology, or life sciences

High school diploma or equivalent

Job description

Overview

Spherion is hiring Pharma Production Technicians in Indianapolis, IN (Park 100 area). The position works Monday through Friday, 7:00 AM – 3:30 PM, with pay ranging from $27 to $30 per hour. It is a mid‑level role in the aseptic filling group of the Manufacturing department, requiring experience and training to produce pharmaceuticals under GMP conditions.

Responsibilities

• Become certified for entry into the GMP cleanroom to perform sanitization, stock/replenish supplies, equipment setup, and aseptic filling operations.
• Execute aseptic fill processes using batch records and SOPs.
• Verify the calibration of all related equipment and sanitization of supplies to support production.
• Progress in competency of manufacturing procedures, including aseptic and cleanroom areas, component preparation, filling, and capping.
• Operate fill-suit equipment and perform tasks with minimal supervisor direction.
• Provide training for new team members.
• Understand the manufacturing schedule and coordinate tasks to meet it.
• Provide floor leadership in the absence of a supervisor or PT3 technicians.
• Transport and/or dispose of hazardous chemicals.
• Perform all other duties as assigned.
• Immediately notify the supervisor if affected by an infectious disease or open lesions, as these conditions prohibit entering manufacturing areas or handling products.

Skills

• B.S. degree in chemistry, biology, or life sciences (preferred).
• Extensive knowledge of bulk formulation and experience with equipment cleaning, preparation, and assembly.
• Computer skills in Microsoft Office (Word and Excel).

Qualifications

• High school diploma or equivalent.
• Minimum of five years of experience using current Good Manufacturing Practices (GMP) in a regulated pharmaceutical/biotech/diagnostic manufacturing facility.
• Proficient in reading, comprehending, and discussing detailed GMP documentation (batch record instructions, SOPs, etc.).
• Strong attention to detail and arithmetic skills for accurate calculations required in manufacturing instructions.
• Leadership experience in training/ directing others.
• Strong mechanical aptitude and ability to troubleshoot, identify problems, and propose solutions.
• Proficiency in isolator work.
• Physical capability to lift or move up to 25 pounds regularly and stand frequently.

Experience

1–4 years in a regulated manufacturing environment.

Education

High School diploma or equivalent.

Benefits and Pay

Pay is based on education, experience, location, and specific job duties. Benefits may include medical, prescription, dental, vision, AD&D, and life insurance, short‑term disability, and a 401(k) plan, subject to eligibility.

Must Not Be Confined With

Position is not a temporary, temp‑to‑perm, or direct hire opportunity at this time.

Contact

Apply today by emailing your resume to [e-mail].

Equal Opportunity Employer

Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

Accommodation

If you require a reasonable accommodation to make your application or interview experience a great one, please contact [e-mail].

EEO Statement

The election that you are a member of an actual or potential union group is protected. Pushback on the request for admission or for the release of any specific data or information related to your status in that election is prohibited. We will not review your application or other documents, including a resume, for information about your union status that might affect your consideration for employment.