Company

Veranova L PSee more

addressAddressDevens, MA
type Form of workFull-Time
CategoryManufacturing

Job description

Job Description

Company Description

Veranova is a global leader in the development and manufacturing of complex active pharmaceutical ingredients (APIs) for pharma and biotech customers. With deep technical expertise and impressive flexibility, we develop solutions and processes that support and accelerate innovation.


Job Description

Under the direction of the team leader, works on supporting and manufacturing of Active Pharmaceutical Ingredients (APIs). Responsible for performing operations in batch records in accordance with Good Manufacturing Practice (GMP) guidelines, acquiring materials and equipment for use, and completing daily checks. Maintains the manufacturing areas in an audit ready state and compliant with Company Standard Operating Procedures (SOPs), FDA, GMPs, DEA regulations and all local, state, and federal regulations regarding safety, health, and the environment. Assists in the cleaning of the manufacturing areas and process equipment.

Key Responsibilities / Accountabilities

  • Synthesize and purify chemical intermediates or active pharmaceutical ingredients using various chemical techniques such as liquid extractions, distillation, crystallization, rotary evaporation, chromatography, etc.
  • Completes batch records in accordance with FDA, Current Good Manufacturing Practices (cGMP), DEA regulations.
  • Applies cGMP concepts in association with department specific responsibilities.
  • Ensure that all work is performed in compliance with Company Standard Operating Procedures (SOPs).
  • Exhibit an elevated level of safety awareness and adhere to the company safety procedures.
  • Assures all production/support equipment is in proper operating condition and that all production equipment is appropriately labeled with a status tag. Works collaboratively with Maintenance, as appropriate.
  • Always ensures the security and safe handling of all controlled substances. Strictly adheres to all Company and DEA regulations.
  • Ensures a high level of housekeeping appropriate for a pharmaceutical manufacturer and maintain 5S areas.
  • Maintain a clean kilo lab and ensure equipment is cleaned after use. Ensure support and work areas meet all requirements for housekeeping.
  • Effectively communicates with QC Testing group regarding timing and prioritization of in-process sample requirements.
  • Ensures that waste is appropriately characterized, labeled, stored, and disposed of in compliance with all Company, state, and federal regulations. Works collaboratively with Environmental, Health & Safety, as appropriate.
  • Operate material handling equipment, such as forklift, drum dollies, hoists, etc.
  • Responsible for reporting all near misses, accidents, and dangerous occurrences through the appropriate Company procedures to ensure an investigation is initiated.
  • Carry out/ take on any other duties which are within the employee’s skills and abilities whenever reasonably instructed.
  • While performing the duties of this job it is required to stand, walk, and use hands to operate objects, tools, or controls; reach with hands or arms; climb, balance, stoop, kneel, or crouch when necessary for job activity.
  • May be required to work 2nd and 3rd shift.
  • Able to lift 50lbs and occasionally lift and or/move more than 100 pounds using available material handling equipment.

Qualifications

  • Existing Veranova employees must meet the internal requirements.
  • Associate degree or equivalent minimum 2 years of experience in STEM field
  • High School Diploma and/or Pharmaceutical Certification or equivalent required with minimum 2 years’ experience.
  • B. Sc with minimum 1 year experience in chemistry/pharmaceutical field or equivalent.
  • Ability to apply scientific and/or technical knowledge in the performance of job duties.
  • Demonstrate attention-to-detail, problem solving, and ability to multi-task.
  • Good written and verbal communication.
  • Experience participating in a teamwork environment. Experience with Microsoft Office and other job-related software
  • Solid understanding of GMP.
  • Prior basic production laboratory skills
  • Experience working in a production Kilo-Lab or GMP production experience is a plus.
  • Ability to read, analyse, and interpret English-language.
  • Ability to write clearly and neatly.
  • Demonstrate ability to exercise good judgment and make decision with guidance from senior team members or supervisor.
  • Good understanding of Microsoft Office
  • Good written and verbal communication skills
  • Experience communicating effectively to peers and supervisors.
  • Ability to work independently and in a team environment.

Additional Information

All your information will be kept confidential according to EEO guidelines.

Veranova is an Equal Opportunity Employer. It is the policy of Veranova to provide equal employment access and opportunity to all persons regardless of age, race, color, national origin, religion, sex, sexual orientation, gender identity and/or expression, physical or mental disability, genetic information, citizenship, marital status, veteran status, or any other characteristic protected by federal, state, or local law.

All applications are carefully considered, and your details will be stored on our secure Application Management System. This is used throughout Veranova for the selection of suitable candidates for our vacancies as they arise. Veranova respects your privacy and is committed to protecting your personal information. For more information about how your personal data is used please view our privacy notice.

Refer code: 9131668. Veranova L P - The previous day - 2024-04-25 06:27

Veranova L P

Devens, MA
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