USA – Manufacturing Associate Position Available In Walton, Georgia

USA

• Manufacturing Associate#25-58140
  Social Circle, GA
  All On-site Job Description

Schedule:

2-2-3 Rotating 12HR
Day Shift 6:00AM-6:30PM

• Primary Duties
• The role is responsible for executing all processes in production while strictly adhering to cGMP,
  environmental health and safety guidelines and any other related regulations which could apply.

He/She is expected to fully participate in both departmental projects and any quality working teams
which may be applicable. He/She initiates new documents for procedures which are simple in nature
and may also make minor revisions to existing documents. The incumbent can troubleshoot simple
existing procedures. He/She may demonstrate procedures as a part of a training session and may
schedule department or process activities which could involve coworkers.

• Responsibilities
• Prepare media and buffer solutions.

Operate Clean-in-Place (CIP) and Steam-in-Place systems.
Assemble and operate filtration systems.
Operate general production equipment (such as pH and conductivity meters, autoclave,
portable mixers, etc.).
Monitor and record critical process parameters.
Complete all relevant paperwork following GDP/GMP guidelines.
Perform routine maintenance and cleaning of production equipment to maintain in GMP
fashion.
Perform sampling using aseptic techniques.
Participate on Continuous Improvement Teams.
Receive and distribute supplies into production areas as necessary.
Train and mentor other team members.
Revise and review pertinent documentation as appropriate.
Assist in troubleshooting process problems and responding to alarms.
May perform other duties as assigned.

• Education and Experience Requirements
• Requires high school diploma or GED plus 1+ years of related experience or
  associate degree or higher with no prior experience required.
• Key Skills, Abilities, and Competencies
• Incumbent must be proficient in a variety of mathematical disciplines and be able to work
  with both the metric and USA standards of measurement.
• Must be able to read and follow detailed written instructions and have good verbal/written
  communication skills.
• Good computer skills, knowledge of Microsoft Word and Excel.
• Knowledge of cGMP manufacturing.
• Knowledge of basic laboratory and pharmaceutical production equipment including but
  not limited to: autoclaves, process tanks, incubators, analytical equipment and CIP/SIP
  systems.
• Knowledge of basic chemical and biological safety procedures.
• Good interpersonal skills and be able to work effectively and efficiently in a team
  environment.
• Other Job Requirements
• Must be able to carry up to 25 lbs., lift up to 50 lbs., and push/pull ? 100 lbs. (with the
  assistance of material handling equipment).
• Must be able to stand for extended periods of time over an entire 8 or 12-hour shift.
• Must be able to climb ladders and stairs while wearing special gowning.
• May require bending, twisting, reaching overhead, and/or squatting motions to perform
  certain tasks.
• Must be able to work in controlled environments requiring special gowning.

Will be
required to follow gowning requirements and wear protective clothing over the head, face,
hands, feet and body.
No make-up, jewelry, contact lenses, nail polish or artificial fingernails may be worn in the manufacturing environment.
Will work in a cold, wet environment.
Must be able to work multiple shifts, including weekends. Must be able to work overtime
as required.
May be required to work in a confined area.
Some Clean Room and cool/hot storage conditions.
May require immunization before performing work within the manufacturing area.

EEO:

“Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of

• Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.

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