Sr. Pharmaceutical Manufacturing Technician - 3rd Shift
About the role
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. The Senior Manufacturing Technician is accountable for results in a fast-paced environment and assists with the manufacturing of drug products (parenteral or solid dosage) for commercial distribution and clinical trials. The Sr. Manufacturing Technician assists with the operation of manufacturing processing equipment by following standard operating procedures (SOPs) and batch records in accordance with regulatory agencies and current Good Manufacturing Practices (cGMPs). The Sr. Manufacturing Technician employs acceptable techniques while working in manufacturing environments, including PPE gowning. The Sr. Manufacturing Technician works collaboratively to support other manufacturing areas as required.
Responsibilities
- Follows applicable SOPs and cGMPs to perform assigned duties and tasks.
- Ensures timely completion and compliance with cGMP and all other relevant company training requirements.
- Assists with applicable manufacturing techniques and technologies per SOPs and cGMPs.
- Assists with manufacturing technologies and operation of manufacturing and material handling equipment.
- Documents activities in real time on controlled documentation and legibly, per SOPs and cGMPs.
- Performs in-process testing, weight checks, component counting and basic math calculations.
- Performs cleaning of rooms, tools and equipment.
- Assists with other manufacturing areas as required.
- 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, Compounding, Aseptic filling, Capping.
Qualifications
- High school diploma or GED required.
- Associate’s degree or technical certification in a related field is preferred.
- 5+ years of GMP and prior pharmaceutical work experience required.
- Up to 5% domestic travel.
Skills
- Excellent verbal and written communication and documentation skills.
- Excellent detail orientation and organizational skills.
- Excellent problem-solving and basic trouble‑shooting ability.
- Ability to perform basic math calculations.
- Ability to read and comprehend detailed written instructions.
- Ability to move materials throughout the facility using appropriate methods and equipment.
- Proficiency in basic computing skills.
- Awareness of or prior experience with cGMP practices and procedures preferred.
Requirements
While performing the duties of this job, the employee is regularly required to stand; use hands to finger, handle, or feel; reach with hands and arms; talk or hear and smell. The employee is frequently required to walk; climb or balance and stoop, kneel, crouch, or crawl. The employee is occasionally required to sit. The employee must regularly lift and/or move up to 25 pounds, frequently lift and/or move up to 50 pounds, occasionally lift and/or move up to 75 pounds and occasionally lift and/or move over 75 pounds with assistance. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus. While performing the duties of this job, the employee is frequently exposed to moving mechanical parts, fumes or airborne particles and toxic or caustic chemicals. The employee is occasionally exposed to wet and/or humid conditions; high, precarious places; risk of electrical shock and vibration. The noise level in the work environment is usually moderate. The employee will be required to wear the appropriate personal protective equipment for specific job duties to be performed. Such personal protective equipment may include, but not limited to safety eyewear, hearing protection, various types of respirators/breathing apparatus, lab coats, full protective body coverings, various types of gloves, etc. The use of tight-fitting respirators limits facial hair for proper protection. Based on product, the use of PAPR or supplied air respirator may be required. Regulations may require employees to participate in routine medical surveillance. Other tasks involving elevated work may require the use of a body harness and lanyard. Additionally, the employee may be required to operate an industrial vehicle.
Schedule
On‑site expectations: 100% on‑site position in Charleston, SC. 3rd Shift: Sunday – Thursday, 11:00 pm – 7:30 am.