In person

MOU status: DoD MOU current through April 2, 2027.

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At a glance

Programs: 3
Locations: 3
States served: 1

Delivery: In person (3)
Program length: Not stated (2), 12 to 20 weeks (1)
Program type: Job Training Program (3)
Branches accepted: Air Force, Army, Coast Guard, Marine Corps, Navy, Space Force

Counts are computed from the DoD program listings below -- a provider with several programs can appear more than once in each count.

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Programs

Manufacturing Associate I - Job Training Program

Detailed listing

Delivery: In person source value: In-Person
Length: About 13 to 17 weeks source value: 91 - 120 days
Type: Job Training Program
Branches: Air Force, Army, Coast Guard, Marine Corps, Navy, Space Force
Career field: Production

Summary

MANUFACTURING ASSOCIATE I GENERAL DESCRIPTION: Entry level position for persons to manufacture commercial scale batches.

What the work involves

KEY DUTIES: • Production, filling and inspection of pharmaceutical formulations. • Assist with facility cleaning and operational maintenance. • Assist with facility and process validations as required. • Perform aseptic production operations and validations. • Assist with environmental and water system monitoring as required. • Assist with clean room sanitization as required. • Assist with RCRA and safety inspections as required. • Document all work as required by CGMPs on a timely basis. • Read and follow all Company SOPs and guidelines. • Abide by all safety requirements as defined by the company. • Other tasks as assigned by team leader.SKILLS/ABILITIES: • Basic knowledge of the Scientific Method • Basic math skills, including simple algebra • Basic knowledge of and adherence to current GMP. • Basic knowledge of chemistry and biology. • Basic knowledge of steam/dry heat sterilization theories. • Basic knowledge of HAZCOM, RCRA and other Safety requirements. • Basic level of mechanical aptitude. • Good documentation skills. • Ability to lift / move 40 lbs. Overhead. • Ability to learn how to operate all types of production equipment (I.e. Autoclave, Honeywell DCS panels, CIP system, Dry Heat Oven, Process Waste system, etc.). • Ability to read, understand and accurately follow company SOPs and guidelines.PERSONAL ATTRIBUTES: • Detail oriented. • Willing to learn new tasks, skills. • Works well in a team environment. • Responds quickly to assignments. • Readily adapts to changing job duties. • Positive attitude. • Displays understanding of and promotes company and customer objectives.EDUCATION AND EXPERIENCE: • High School diploma or equivalent. • 0-1 years experience in a sterile pharmaceutical operation.

Locations

Wilmington, OH

Quality Control Analyst I - Job Training Program

Partial listing

Delivery: In person source value: In-Person
Length: Duration not stated The DoD listing does not state a length for this program. Ask the organization directly.
Type: Job Training Program
Branches: Air Force, Army, Coast Guard, Marine Corps, Navy, Space Force

Summary

QC Analyst I must have broad knowledge of all the techniques within the laboratory required for the routine support of the microbiology laboratory operations. In this role the Analyst will be a fully functional member of the team responsible for testing, data entry and occasional review of data for finished product, in-process samples, stability samples, clinical materials and raw material release in a cGMP regulated environment

What the work involves

Major Responsibilities: • Execution of microbiological tests including but not limited to bioburden, LAL, growth promotion, sterility, particulate profiling and microbial identification of bulk, raw materials, in-process material, components, clinical materials and finished product • Review and data entry for testing results following GMP regulations into the electronic data management systems • Participate in non-routine projects, validations and method development to meet departmental and individual goals • The employee will be required to participate in an on call schedule for various shift, holiday, or weekend work as needed. Preferred Qualifications: • Experience with the execution of test methods for sterile and non-sterile drug products, raw materials, components and in-process testing. This includes the methods described in USP Chapters 61, 62, 71, 85, 788 and relevant informational chapters • Critical thinker, ability to identify issues and work quickly to bring resolution • Capable of managing/coordinating multiple priorities in a dynamic environment, while maintaining a professional demeanor • Understand common microbiological test instrumentation • Excellent organizational, planning and scheduling skills • Good verbal and written communication skills • The successful employee will have the ability to function in a microbiological laboratory environment; the employee should have no inhibitions regarding safely handling microorganisms present in the laboratory, aseptic gowning, and no health conditions that would prevent them from doing so Preferred Technical Abilities and Personal Skills • Ability to work safely; seek out and encourage safe practices • Ability to focus attention to details and ensure high quality work • Ability to cope with a rapidly changing work environment • Self-starter that takes initiative to do work with minimal supervision • Time management skills Other Preferred Characteristics • Commitment to teamwork • Commitment to continuous improvement • Effective communication with co-workers and supervisors Education and Experience: • Bachelor's in science, preferably in Biology / Microbiology / Biotechnology or Biochemistry, required • For QC Analyst I role, 1+ year experience in pharmaceutical manufacturing or contract testing laboratory required Physical Requirements: • Employee must be able to pass a vision exam prior to employment and annually thereafter. • This job requires a large amount of physical activity • Walking, lifting, pushing and pulling carts, reaching, climbing, and bending are all required • Steel toe shoes, scrubs, safety glasses, and other PPE equipment must be worn based on job being performed Alkermes, Inc. is an equal employment opportunity employer and does not discriminate against any applicant because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, gender expression and identity, disability, genetic information, veteran status, military status, application for military service or any other class protected by state or federal law.

Locations

Wilmington, OH

Quality Control Analyst III - Job Training Program

Partial listing

Delivery: In person source value: In-Person
Length: Duration not stated The DoD listing does not state a length for this program. Ask the organization directly.
Type: Job Training Program
Branches: Air Force, Army, Coast Guard, Marine Corps, Navy, Space Force

Summary

QC Analyst III must have broad knowledge of all the techniques within the laboratory required for the routine support of the microbiology laboratory operations. In this role the Analyst will be a fully functional member of the team responsible for testing, data entry and occasional review of data for finished product, in-process samples, stability samples, clinical materials and raw material release in a cGMP regulated environment.

What the work involves

Major Responsibilities: • Execution of microbiological tests including but not limited to bioburden, LAL, growth promotion, sterility, particulate profiling and microbial identification of bulk, raw materials, in-process material, components, clinical materials and finished product • Review and data entry for testing results following GMP regulations into the electronic data management systems • Perform laboratory investigations for out of specification and/or out of trend results in conjunction with management • Write change controls and work orders for systems and instrumentation changes • Creation/Revision of SOP’s, and other documents required to support testing and ensure compliance • Participate in non-routine projects, validations and method development to meet departmental and individual goals • The employee will be required to participate in an on call schedule for various shift, holiday, or weekend work as needed. Preferred Qualifications: • Experience with the execution of test methods for sterile and non-sterile drug products, raw materials, components and in-process testing. This includes the methods described in USP Chapters 61, 62, 71, 85, 788 and relevant informational chapters • Critical thinker, ability to identify issues and work quickly to bring resolution • Capable of managing/coordinating multiple priorities in a dynamic environment, while maintaining a professional demeanor • Understand common microbiological test instrumentation • Excellent organizational, planning and scheduling skills • Good verbal and written communication skills • Experience of Thermo Sample Manager LIMS or other applicable LIMS systems • The successful employee will have the ability to function in a microbiological laboratory environment; the employee should have no inhibitions regarding safely handling microorganisms present in the laboratory, aseptic gowning, and no health conditions that would prevent them from doing so Preferred Technical Abilities and Personal Skills • Ability to work safely; seek out and encourage safe practices • Ability to focus attention to details and ensure high quality work • Ability to cope with a rapidly changing work environment • Self-starter that takes initiative to do work with minimal supervision • Time management skills Other Preferred Characteristics • Commitment to teamwork • Commitment to continuous improvement • Effective communication with co-workers and supervisors Education and Experience: • Bachelor's in science, preferably in Biology / Microbiology / Biotechnology or Biochemistry, required • For QC Analyst III role, 3+ year experience in pharmaceutical manufacturing or contract testing laboratory required Physical Requirements: • This job requires a large amount of physical activity • Walking, lifting, pushing and pulling carts, reaching, climbing, and bending are all required • Steel toe shoes, scrubs, safety glasses, and other PPE equipment must be worn based on job being performed

Locations

Wilmington, OH

Where this provider operates

OhioWilmington

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Where this comes from

Source is the Department of Defense SkillBridge directory, filtered to Alkermes. HiredTroops republishes it and adds the plain-language notes. We do not screen, rank, or endorse organizations, and we take nothing from them.

Last checked August 23, 2026, which is older than our normal weekly refresh.

Confirm current program status with the organization and with your command before you commit. This directory is not affiliated with or endorsed by the Department of Defense.