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Alcami

Pharmaceutical and biologics CDMO services

Validation Engineer 1

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timePepperell, MA, USA$32 - $38 /hr

About the Job

Requirements

  • A BA/BS in a technical or science-related field of study, or an HSD/GED, technical training, or an associate’s degree combined with mechanical aptitude or relevant industry experience.
  • A valid driver’s license is required.
  • Strong working knowledge of information technology concepts, strategies, and methodologies.
  • Proficiency with Microsoft Office, including Word, Excel, and PowerPoint.
  • Strong mechanical skills.
  • Strong reporting, organizational, and interpersonal skills.
  • Ability to multitask and perform tasks with high quality and accuracy.

Responsibilities

  • Perform pre- and post-validation verification on test equipment.
  • Create and execute validation protocols, procedures, and final reports, and perform validation projects.
  • Perform peer review of validation reports.
  • Learn and execute troubleshooting strategies in the field.
  • Write and document validation reports.
  • Write to clients and work with them to resolve deviations.
  • Maintain pertinent project information records, including project cost reconciliation.
  • Relay opinions or interpretations of results to customers.
  • Perform other duties as assigned.
  • Travel during the day to client sites, with overnight travel as project requirements dictate.
  • Work on-site and provide occasional off-shift, overnight, or weekend coverage as needed to accommodate schedules or project timelines.

Desired Qualifications

  • Validation experience or experience working in a good manufacturing practice-regulated environment, including working knowledge of ISO 9001, ISO 17025, good manufacturing practice, good laboratory practice, GAMP 5, and 21 CFR Part 11.

About the Company

Alcami

Pharmaceutical and biologics CDMO services

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
Not listed
Total funding
Not listed
Headquarters
Pepperell, MA
Founded
1984

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