Job Title: QA Specialist I
Location (On-site Remote or Hybrid): Scarborough ME (onsite)
Contract Duration: Contract until 12/31/2026
Work Hours: 8:00AM - 5:00PM
Description:
This position is NonExempt. Hours over 40 will be paid at Time and a Half. Assures the quality of manufactured products and processes per standard operating processes(SOPS) and GMP (Good Manufacturing Practices). Degree not required
The position of Quality Assurance Specialist I is within our Infectious Disease Business Unit located at Scarborough this role you will under basic direction and supervision provide support for product quality assurance process improvements and all quality system programs at the Scarborough Site.
RESPONSIBILITIES:
The following activities may be assigned as applicable:
- Review production batch records (DHRs) for accuracy and completeness in order to approve intermediate products for use in production. Review finished goods batch records. Report all deviations in these records and assure they have been addressed and resolved prior to issuing approval.
- Conduct spot-check inspections/audits of production operations
- Write Standard Operating Procedures (SOPs) as necessary
- Assist in testing of complaint samples and stability samples and report results out of acceptance limits
- Initiate Quality Incidents (QI)
- Provide backup to other Quality Specialists
- May organize the long-term stability program and be responsible for administering the sample retention program
- May administer or support the site s current electronic Document Control System (eDCS)
- May administer or support the site s current electronic Quality Incident and CAPA tracking system.
- Other duties may be assigned.
BASIC QUALIFICATIONS EDUCATION:
- Bachelors Degree in Chemistry Biology Life Science or other related technical field in a scientific or technical area or the equivalent combination of education and experience.
- 1 years in Quality Assurance role or similar support for manufacturing.
PREFERRED QUALIFICATIONS:
Prior experience in a Quality Assurance role or similary support role in the medical device industry
COMPETENCIES:
- Knowledge of spreadsheet software and word processing software
- Ability to follow procedures and accurately document results
- Ability to understand the manufacturing processes of Company products and ability to recognize deviations from approved documented procedures
- Ability to read and interpret documents such as safety rules operating and maintenance instructions and procedure manuals.
- Ability to interpret a variety of instructions furnished in written oral diagram or schedule form
- Ability to write routine reports and correspondence
- Ability to apply mathematical concepts such as fractions percentages ratios and proportions to practical situations
- Attention to detail
Job Title: QA Specialist I Location (On-site Remote or Hybrid): Scarborough ME (onsite) Contract Duration: Contract until 12/31/2026 Work Hours: 8:00AM - 5:00PM Description: This position is NonExempt. Hours over 40 will be paid at Time and a Half. Assures the quality of manufactured product...
Job Title: QA Specialist I
Location (On-site Remote or Hybrid): Scarborough ME (onsite)
Contract Duration: Contract until 12/31/2026
Work Hours: 8:00AM - 5:00PM
Description:
This position is NonExempt. Hours over 40 will be paid at Time and a Half. Assures the quality of manufactured products and processes per standard operating processes(SOPS) and GMP (Good Manufacturing Practices). Degree not required
The position of Quality Assurance Specialist I is within our Infectious Disease Business Unit located at Scarborough this role you will under basic direction and supervision provide support for product quality assurance process improvements and all quality system programs at the Scarborough Site.
RESPONSIBILITIES:
The following activities may be assigned as applicable:
- Review production batch records (DHRs) for accuracy and completeness in order to approve intermediate products for use in production. Review finished goods batch records. Report all deviations in these records and assure they have been addressed and resolved prior to issuing approval.
- Conduct spot-check inspections/audits of production operations
- Write Standard Operating Procedures (SOPs) as necessary
- Assist in testing of complaint samples and stability samples and report results out of acceptance limits
- Initiate Quality Incidents (QI)
- Provide backup to other Quality Specialists
- May organize the long-term stability program and be responsible for administering the sample retention program
- May administer or support the site s current electronic Document Control System (eDCS)
- May administer or support the site s current electronic Quality Incident and CAPA tracking system.
- Other duties may be assigned.
BASIC QUALIFICATIONS EDUCATION:
- Bachelors Degree in Chemistry Biology Life Science or other related technical field in a scientific or technical area or the equivalent combination of education and experience.
- 1 years in Quality Assurance role or similar support for manufacturing.
PREFERRED QUALIFICATIONS:
Prior experience in a Quality Assurance role or similary support role in the medical device industry
COMPETENCIES:
- Knowledge of spreadsheet software and word processing software
- Ability to follow procedures and accurately document results
- Ability to understand the manufacturing processes of Company products and ability to recognize deviations from approved documented procedures
- Ability to read and interpret documents such as safety rules operating and maintenance instructions and procedure manuals.
- Ability to interpret a variety of instructions furnished in written oral diagram or schedule form
- Ability to write routine reports and correspondence
- Ability to apply mathematical concepts such as fractions percentages ratios and proportions to practical situations
- Attention to detail
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