Careers | Accupac

Careers

Chem Weigh Supervisor

Job Title
Chem Weigh Supervisor
Job ID
27739793
Location
Souderton, PA,  
Other Location
Description

Accupac, Inc.

Job Description

Title:  Supervisor, Chem Weigh                                                                                              
Location / Department:  Chem Weigh
Reports To:  Manufacturing Manager
FLSA Status:  Exempt
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Basic Job Functions:
Responsible to lead the Chemweigh staff to assure that all personnel are working to accomplish duties as outlined in their job descriptions.  Responsible for leading initiatives relating to Chemweigh in support of schedule adherence.

Essential Functions of the Job:
  • Direct Chemweigh staff on priorities to support the production schedule.
  • Participate in any internal or external meetings as related to Chemweigh group.
  • Assist upper management as needed. 
  • Direct Chemweigh personnel to ensure that all job functions are being met.
  • Ensure Chemweigh department has all essential tools needed to perform daily tasks.
  • Promote and maintain a safe, accident free, and healthy work environment.
  • Maintain and enforce general safety policies and procedures followed by company and plant personnel in compliance with state, local and federal Occupational Administration (OSHA) regulations and requirements.
  • Consult within the department on design and use of equipment, fire prevention, and safety programs.
  • Oversee all accident investigations.
  • Lead all Chemweigh personnel performance reviews and disciplinary actions as needed with Manufacturing Management consultation.
  • Oversee, approve, maintain, and coordinate training programs related to the Chem- weigh department.
  • Regularly review raw material status and report any discrepancies that may impact production.
  • Ensure department is cleaned and maintained.  Submits work orders as needed.
  • Work with validation department to schedule equipment calibrations.
  • Complete Preventative Maintenance on equipment as needed.
  • Ensure department is stocked with tools and supplies needed for all Chemweigh functions.  Order supplies as needed.
  • Oversee transfer of raw materials between Accupac sites as needed.
  • Perform all other duties as assigned.


Minimum Requirements of the Job:
  • Possess computer skills sufficient to operate a PC and interface with a mainframe.
  • Possess analytical ability sufficient to interpret reports.
  • Possess writing skills sufficient to interpret reports.
  • Possess oral communications skills sufficient to conduct meetings and small group presentations.
  • Able to type, copy, fax and file in binders as well as traditional files.
  • Able to use current company software for spreadsheets, word processing, etc.
  • Able to wear a tight-fitted negative pressure air-purifying respirator.  Employees must be clean shaven with no facial hair to be able to daily use this type of respirator.
 

Preferred Qualifications:

  • Possess basic knowledge of planning, scheduling, inventory control, and cGMP's.

Physical Requirements:
  • Must be able to travel via car between facilities as needed.
  • Able to walk/stand on concrete floors for up to three (3) hours per day and for long distances.
  • Able to sit for 80-90% of the workday.
  • Able to bend/stoop repeatedly.
  • Able to climb step stools and maintain balance.
  • Able to lift/carry items up to 25 pounds.
  • Able to push/pull items up to 50 pounds.
  • Able to hear/execute speech in person and over the telephone.
  • Able to hear phones ring, alarms sound through ambient noise and everyday conversation. 
  • Possess good peripheral vision.

Supervisory Responsibilities:  Requires supervising numerous Chem-weigh and material handling personnel.

Travel:  May require travel between various Accupac sites.

Education and/or Experience: Must have a high school diploma or GED, College preferred.  Requires experience in a pharmaceutical manufacturing cGMP environment
Required Skills

Education and/or Experience: Must have a high school diploma or GED, College preferred. Requires experience in a pharmaceutical manufacturing cGMP environment

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