Full-Time

Manufacturing Technician 3

Sterile Injection

Updated on 9/17/2026

Deadline 8/17/27
Alcami

Alcami

51-200 employees

Pharmaceutical and biologics CDMO services

No salary listed

Morrisville, NC, USA

Remote

100% on-site; 12-hour rotating night shift (7:00 p.m. to 7:00 a.m.).

Bachelor's, Associate's

Category
Biology & Biotech (1)
Required Skills
Microsoft Office
GMP

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Requirements
  • A high school diploma or GED is required.
  • Four to six or more years of relevant experience are required, including a strong background in sterile or aseptic manufacturing or drug substance manufacturing.
  • Prior experience in a current Good Manufacturing Practice pharmaceutical manufacturing environment is required.
  • Prior pharmaceutical or contract development and manufacturing organization experience is required.
  • Ability to execute tasks with minimal oversight while giving guidance to the team is required.
  • Ability to operate, troubleshoot, and maintain complex manufacturing equipment is required.
  • Strong analytical, problem-solving, detail-orientation, and organizational skills are required.
  • Ability to train and mentor other team members effectively is required.
  • Ability to perform basic mathematical calculations is required.
  • Ability to read and comprehend detailed written instructions and apply them during execution is required.
  • Ability to move materials throughout the facility using appropriate methods and equipment is required.
  • Ability to use appropriate personal protective equipment based on the product, including a powered air-purifying respirator or supplied-air respirator, is required.
  • Basic computer skills, including Microsoft Office, and familiarity with electronic documentation systems are required.
  • Ability to meet the stated physical demands, including lifting and moving materials, is required.
  • Ability to have 20/20 vision with or without corrective lenses and pass a color-blind test is required.
  • Ability to wear required personal protective equipment and comply with applicable medical-surveillance requirements is required.
Responsibilities
  • Perform complex manufacturing operations, including setup, operation, and maintenance of equipment used in dispensing, compounding, isolator filling, and visual inspection.
  • Serve as a subject matter expert on compounding and filling processes and equipment, providing guidance and training to other manufacturing employees.
  • Monitor production processes for adherence to standard operating procedures, batch records, and quality standards, making real-time adjustments to maintain product quality.
  • Troubleshoot and resolve complex equipment and process issues to minimize downtime and maintain efficient production flow.
  • Conduct in-process and end-of-process sampling and quality checks.
  • Collaborate with Manufacturing Specialists, Technical Services, Quality Assurance, Engineering, and other cross-functional teams on continuous-improvement initiatives.
  • Contribute to manufacturing readiness and execution by implementing process ideas.
  • Assist with validation and qualification of new equipment and processes.
  • Maintain accurate and detailed production documentation and escalate recommendations for document revisions.
  • Follow standard operating procedures and current Good Manufacturing Practices when performing assigned duties.
  • Complete required company training on time and in compliance with current Good Manufacturing Practices.
  • Legibly document activities in real time on controlled documentation according to standard operating procedures and current Good Manufacturing Practices.
  • Perform in-process sampling, weight checks, component counting, and basic mathematical calculations.
  • Perform in-process and finished-product visual inspections.
  • Clean rooms, tools, and equipment before and after use.
  • Perform material handling, dispensing, compounding, and filling activities right the first time.
  • Follow general instructions for routine work and detailed instructions for new projects or assignments.
  • Follow safety requirements and lead by example in maintaining a safety-first culture.
  • Work occasional hours outside the scheduled shift, including weekend work, based on business needs.
  • Perform equipment and component preparation and sterilization, including filter-integrity testing, autoclaving, and parts wrapping.
  • Perform compounding, vial washing and depyrogenation, aseptic filling, stoppering, capping, lyophilization, visual inspection, facility cleaning and sanitation, and documentation review.
  • Assist with other manufacturing areas as required and perform other assigned duties.
  • Travel domestically up to 5%.
Desired Qualifications
  • An associate’s or bachelor’s degree is preferred.

Alcami is a contract development and manufacturing organization supporting pharmaceutical and biologics companies from early development through commercial production. Services span drug product manufacturing (sterile fill-finish and oral solid dose), analytical and microbiology lab testing, and cGMP storage with validation and environmental monitoring. What sets Alcami apart is its integrated, end-to-end capabilities across the development lifecycle. The goal is to help pharma and biotech partners deliver safe, high-quality therapies to patients.

Company Size

51-200

Company Stage

N/A

Total Funding

N/A

Headquarters

Pepperell, Massachusetts

Founded

1984

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Simplify Jobs

Simplify's Take

What believers are saying

  • Alcami acquired Tjoapack on May 5, 2026, expanding packaging reach into the Netherlands.
  • January 19, 2026 Durham facility purchase deepens biologics capacity for advanced services.
  • Revelio reported 1,038 employees in March 2026, showing hiring despite CEO turnover.

What critics are saying

  • February 6, 2026 FDA 483 at Charleston flagged sterile manufacturing controls and investigations.
  • Tjoapack integration strains management through 2026, with packaging line delivery only in 2027.
  • A sterile quality failure could shut Charleston operations and imperil Alcami's CDMO credibility.

What makes Alcami unique

  • Patrick Walsh keeps Alcami founder-level operator continuity after January 2025 CEO transition.
  • Durham RTP expansion adds fifth GMP fill-finish line and broad biologics analytical capacity.
  • Six-site U.S. GMP storage network gives Alcami integrated storage, testing, and manufacturing.

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Benefits

Remote Work Options

Company News

PR Newswire
Jan 13th, 2025
Alcami Announces Ceo Transition

Long time industry leader, Chairman of the Board Patrick Walsh replaces CEO Bill Humphries DURHAM, N.C., Jan. 13, 2025 /PRNewswire/ -- Alcami Corporation ("Alcami"), a leading contract development and manufacturing organization (CDMO), today announced the resignation of Bill Humphries. Alcami's Board Chair and former Chief Executive Officer Patrick Walsh will serve as Interim CEO, ensuring the continuation of smooth operations and a strong client-centric approach from a proven industry veteran

PR Newswire
Jul 23rd, 2024
Alcami Unveils New Conditions And Services At State-Of-The-Art Pharma Storage Facility In Garner

"Alcami's new facility is well positioned to fill previously unmet market demand," said Laurent Boer, President, Alcami Pharma Storage and Services. "The pipeline of complex medicines – exactly the type of ground-breaking products that life science companies in RTP work on – is only increasing. The biopharmaceutical materials and products in these drugs require very specific warehouse conditions that this new facility provides. But what truly sets us apart as a CDMO is our ability to offer a comprehensive pharma storage network paired with seamless access to our integrated laboratory and manufacturing services. From development to delivery, Alcami has the capabilities to care for and secure product within our own network, reducing risk and streamlining efficiency."After opening in January with controlled/ambient storage, the facility can now accept shipments for an extensive range of storage conditions, including stability chamber storage, refrigerated storage, freezer, ultra-low freezer, and cryogenic storage (LN2) as well as custom conditions. In addition, the site now offers a full suite of materials management and support services that facilitate the full product development, storage, and commercialization journey, including onsite aliquoting/sampling in grade C sampling booths, refrigerated transport, labeling, cycle counting/inventory management, custom kitting, and reference standards management.The new central North Carolina facility adjacent to the Research Triangle Park expands Alcami's high-quality, secure GMP storage network to six U.S

Contract Pharma
Dec 15th, 2021
alcami acquires Masy Systems Inc.

Alcami Corp., a pharmaceutical and biotech contract development and manufacturing organization ( CDMO ), has completed the acquisition of Masy Systems Inc., a provider of cGMP biostorage and pharma support services.

PR Newswire
Dec 15th, 2021
AAIPharma Services Corp. acquired Masy Systems Inc. on Dec 15th 21'.

Alcami Corporation, a leading pharmaceutical and biotech contract development and manufacturing organization (CDMO), announced today it has completed the acquisition of Masy Systems Inc. ("Masy" or "Masy BioServices"), a preferred provider of cGMP Biostorage and pharma support services.

Daily Times Chronicle
Dec 1st, 2021
Masy Systems Inc. launches SenseAnywhere modules

Masy BioServices announces the launch of innovative SenseAnywhere modules.