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Pharmaceutical Manufacturing Technician II - 2nd Shift

Job in Sumter, Sumter County, South Carolina, 29153, USA
Listing for: Alcami Corporation
Per diem position
Listed on 2026-07-15
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Validation Engineer, Production QC/QA, Manufacturing & Industrial Operations
Salary/Wage Range or Industry Benchmark: 52000 - 72000 USD Yearly USD 52000.00 72000.00 YEAR
Job Description & How to Apply Below

At Alcami, we deliver reliable solutions that unlock the potential of transformative medicines from discovery to commercialization, through trusted partnership with our clients, recognized industry expertise and proven regulatory track record.

Job Summary

The Manufacturing Technician II (Compound/Fill/Finish) is accountable for results in a fast‑paced environment and assists with manufacturing of sterile injectable products in vial and syringe configurations for clinical/commercial distribution. This role performs advanced production tasks involving compound, fill and finish processes for sterile injectable pharmaceutical products executed via aseptic isolator technology. It requires technical expertise in aseptic processes, single‑use components, troubleshooting, and maintaining quality and compliance with Good Manufacturing Practices (GMP).

The technician operates manufacturing processing equipment following SOPs and batch records, ensuring adherence to regulatory agencies, current Good Manufacturing Practices (cGMPs), Good Documentation Practices (GDP), and all training requirements while working in PPE‑gowned environments.

On‑Site Expectations
  • 100% on‑site position.
  • 2nd Shift: Monday - Friday, 3:00 pm - 11:30 pm.
Responsibilities
  • Learns and executes manufacturing operations including setup, operation, and maintenance of equipment used in dispensing, compounding, filling (isolators), and visual inspection.
  • Becomes a subject matter expert (SME) on compounding/filling processes and equipment.
  • Performs production processes with adherence to SOPs, batch records, quality standards, and minimally contributes deviations to maintain product quality.
  • Conducts in‑process and end‑of‑process sampling/quality checks, ensuring all manufactured products meet rigorous standards.
  • Identifies inefficiencies and escalates to area supervision in real time to support continuous process improvement.
  • Maintains accurate and detailed production documentation, completed legibly with minimal errors and escalates recommendations to drive document revisions.
  • Ensures timely completion and compliance with cGMP and all other relevant company training requirements.
  • Demonstrates technical ability in general manufacturing technologies and utilizes technologies per SOPs and cGMPs.
  • Performs in‑process sampling, weight checks, component counting and basic math calculations.
  • Performs in‑process inspection and finished product visual inspection.
  • Performs cleaning of rooms, tools, and equipment before and after use.
  • Assists with other manufacturing areas as required.
  • Performs activities right the first time in material handling/dispensing, compounding, and filling.
  • Follows general instructions on routine work and detailed instructions on new projects or assignments.
  • Follows all safety requirements and leads by example a safety‑first culture.
  • Works occasional hours outside of scheduled shift based on business needs, which may include weekend work.
  • Other duties as assigned.
Manufacturing Technologies for Sterile Liquids
  • Equipment and component preparation and sterilization (filter integrity testing, autoclaving, parts wrapping).
  • Compounding.
  • Vial washing/depyrogenation.
  • Aseptic filling/stoppering/capping.
  • Lyophilization.
  • Visual inspection.
  • Facility cleaning/sanitation.
  • Documentation review (batch record, logbooks, etc.).
Qualifications
  • High school diploma or GED is required. Associate or bachelor’s degree preferred.
  • 2‑3+ years’ work experience required.
  • Prior work experience in a cGMP pharmaceutical manufacturing environment required.
  • Previous experience in dispensing, compounding, aseptic filling, or visual inspection highly desirable.
  • Candidates with life sciences or engineering degrees will be considered without manufacturing experience.
Knowledge, Skills, And Abilities
  • Excellent verbal and written communication skills, works collaboratively in a team environment.
  • Proven ability to operate, troubleshoot, and maintain complex manufacturing equipment.
  • Applies job skills, company policies, and SOPs to complete a variety of assignments.
  • Strong detail orientation and organizational skills required.
  • Strong problem‑solving and basic troubleshooting ability required.
  • Ability…
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