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Microbiology Analyst I

Sun Pharmaceutical Industries, Inc.
Posted a day ago, valid for a year
Location

Billerica, MA 01821, US

Salary

$50,000 - $60,000 per annum

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Contract type

Full Time

Paid Time Off
Life Insurance
Disability Insurance
Employee Assistance
Flexible Spending Account

Sonic Summary

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  • The position involves performing GMP testing of raw materials, in-process and finished products, and conducting microbial identification.
  • Candidates should have a BS in Microbiology or relevant experience, with 0-2 years of related experience in the pharmaceutical industry preferred.
  • The anticipated salary range for this role is between $78,000 and $95,160, depending on experience and geographical location.
  • Responsibilities include recording GMP data, interacting with auditors, and maintaining compliance with cGMP standards.
  • The role requires strong communication skills and proficiency in following written SOPs, as well as good computer skills.

Job Summary

Performs GMP testing of raw materials, in-process and finished products, stability samples, and non-routine sample analyses per established procedures and methodology.

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Area Of Responsibility

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  • Record GMP data, monitor and evaluate QC systems and equipment
  • Recommend improvements to procedures, and revise SOPs and GMP documentation as required
  • Interact with internal and external auditors including government agencies and contract manufacturing representatives
  • Perform release, stability, validation and complaint follow-up assays on raw materials, in-process and final products
  • Perform microbial identification related to product and environmental testing
  • Perform sampling of raw materials as required for QC testing
  • Perform routine quality control testing as required and monitors or evaluate systems, equipment (i.e. water systems, environmental chambers, sample collection and testing instruments/equipment)
  • Maintain records in paper based or computer based systems
  • Execute method validation protocols related to product testing
  • Author summary reports for executed method validations
  • Author deviation reports and microbiological assessment reports related to departmental activities and product support
  • Provide technical input on product testing issues and instrumentation/equipment
  • Serve as liaison to service, calibration and technical representatives
  • Conduct and document assay failure and complaint investigations
  • Ensure that laboratory is in cGMP compliance and conduct inspections
  • Other duties as assigned

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Work Conditions:

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  • Lab
  • Office
  • Laminar flow and biosafety hoods
  • Exposure to noise, bio-hazardous (live cultures), and chemicals
  • May entail exposure to radiation within NRC limits
  • Exposure to or use of syringes and needles
  • Exposure to non-hazardous and hazardous chemicals and materials
  • Exposure to biological safety cabinets
  • Requires work in class 100K, 10K or 100 clean room (mask and boots in conformance with environmental dress codes
  • Moderate noise, oven heat, open flame, chemical fume hoods areas requiring wearing appropriate safety equipment (i.e. gloves, lab coat, safety glasses and respirator)

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Physical Requirements:

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  • Stand, sit, walk, use hands and fingers to handle or feel, reach with arms and hands, talk or hear,Ā stoop, kneel, crouch or crawl.
  • Close vision;Ā depth perception; ability to adjust focus
  • Use of repetitive motion
  • Able to operate computer/office machines
  • Lift up to 25 lbs.

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Travel Estimate

Up to 0%

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Education and Job Qualification

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  • BS in Microbiology or relevant experience required

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Experience

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  • 0-2 years related experience in a Pharmaceutical/drug (FDA Regulated) industry preferred
  • Experience in pharmaceutical microbiology and microbiology testing not limited to endotoxin, method validation, sterility, bioburden, microbial identification, growth promotion and environmental monitoring testing; ability to perform standard and non-standard microbiology techniques to analyze product
  • Excellent verbal, written and interpersonal communication skills
  • Proficient at following specific instruction (i.e. written SOPs)
  • Working knowledge of cGMP/GLP
  • Good computer skills including word processing and working with spreadsheets

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The presently-anticipated base compensation pay range for this position is $78,000 to $95,160. Actual base compensation may vary based on a number of factors, including but not limited to geographical location and experience. In addition, this position is part of the Annual Performance Bonus Plan. Employees are eligible to participate in Company employee benefit programs which include medical, dental and vision coverage; life insurance; disability insurance; 401(k) savings plan; flexible spending accounts; and the employee assistance program. Employees also receive various paid time off benefits, including vacation time and sick time.

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Actual base compensation may vary based on a number of factors, including but not limited to geographical location and experience. In addition, this position is part of the Annual Performance Bonus Plan, and may be eligible for the Employees are eligible to participate in Company employee benefit programs which include medical, dental and vision coverage; life insurance; disability insurance; 401(k) savings plan; flexible spending accounts; and the employee assistance program. Employees also receive various paid time off benefits, including vacation time and sick time.

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The compensation and benefits described above are subject to the terms and conditions of any governing plans, policies, practices, agreements, or other materials or documents as in effect from time to time, including but not limited to terms and conditions regarding eligibility.Ā If hired, employee will be in an ā€œat-will positionā€ and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company, or individual department/team performance, and market factors.

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The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of the incumbent(s).

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We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, military or veteran status, generic predisposing characteristics or any other basis prohibited by law.

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Notice to Agency and Search Firm Representatives:

Sun Pharmaceuticals (Sun) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Taro employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Taro. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral.Ā 
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