Drug Manufacturing Specialist

Job Title: Drug Manufacturing SpecialistJob Description

We are seeking an experienced Drug Manufacturing Specialist to join a growing Contract Development and Manufacturing Organization (CDMO). The role is based in Indianapolis, Indiana, with production locations in South Bend, IN, and Bunker Hill, IN. The Specialist will be responsible for the process manufacturing of radiopharmaceutical products, preparation of production materials, supplies, and general production equipment maintenance.

Responsibilities

• Carry out production responsibilities to meet manufacturing schedules.

• Perform chemistry manipulations for production in a GMP environment.

• Ensure regulatory compliance of production protocols within the manufacturing operations.

• Conduct analytical methods and procedures for testing GMP manufactured radiopharmaceutical products.

• Prepare and submit required reports.

• Support and execute deviation reports, Out of Specification (OOS) reports, root cause investigations, and Corrective and Preventive Actions (CAPA).

• Optimize and validate methods and procedures for radiopharmaceutical products.

• Assist with creating Standard Operating Procedures (SOPs) for use in production.

• Assist with the preparation of regulatory submissions.

• Assist with general lab cleaning, supplies, and maintenance.

• Assist with waste management.

• Perform other related duties as assigned.

Essential Skills

• Experience in Laboratory, Chemistry, or Chemical Engineering.

• Background in Radiopharmaceutical or Pharmaceutical Manufacturing.

• Understanding of Quality Control, Nuclear Medicine, and GMP protocols.

• Competence in HPLC, Isotope, and Radioactive material handling.

• Proficiency in Aseptic and Cleanroom procedures.

• Troubleshooting skills for lab equipment and instrumentation.

• Experience in Validation, Instrument Qualification, and Calibration.

• Knowledge of Radiation and Radiopharma processes.

Additional Skills & Qualifications

• Associates degree in chemistry, biochemistry, chemical engineering, or a related field.

• Minimum of 2 years of related experience in a pharmaceutical manufacturing environment, with a preference for radiopharmaceuticals.

• Experience in pharmaceuticals, preferably in a quality or production position.

• Prior experience in a radiopharmaceutical environment is a plus.

• Excellent communication, analytical, computer/PC, and technical writing skills.

• Ability to handle responsibilities in a fast-paced manufacturing environment.

• Demonstrated ability to work as part of a team.

• Thorough understanding of project management.

• Excellent organizational skills and attention to detail.

Work Environment

Candidates will work onsite at the facility located at Grissom Air Force Base in Bunker Hill, IN.

Job Type & Location

This is a Contract to Hire position based out of Bunker Hill, IN.

Pay and Benefits

The pay range for this position is $30.00 - $35.00/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: Medical, dental & vision Critical Illness, Accident, and Hospital 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available Life Insurance (Voluntary Life & AD&D for the employee and dependents) Short and long-term disability Health Spending Account (HSA) Transportation benefits Employee Assistance Program Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in Bunker Hill,IN.

Application Deadline

This position is anticipated to close on Oct 21, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [email protected] for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.