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Quality Control Laboratory Specialist
Job Location:
Job Location:
Manati, us-territories - USA
Monthly Salary:
Not provided by the employer
Monthly Salary:
Posted:
17 June 2026 (30+ days ago)
Posted:
Application Deadline:
14 September 2026
Application Deadline:
Vacancies:
1 Vacancy
Vacancies:
Job Summary
Quality Control Laboratory Specialist
Work Location: Manati Site 100% OnSite
Hours: Mon-Fri 8a-5pm
Paga: 26.78 p/h
Position Summary
The Specialist in this role will be responsible for executing routine testing of complex and non-complex methods on intermediate or finished products a environmental monitoring utility testing raw materials etc. as appropriate for the individual role. They will also support lab operations activities such as housekeeping as required.
Key Responsibilities
Executes routine testing of non-complex/compendial methods environmental monitoring utility testing raw materials etc. as appropriate for the individual role
Perform release/stability testing for complex and non-complex methods on intermediate or finished product
Perform activities to support lab operations such as housekeeping alarm acknowledgement reagent preparation inventory management material and reagent ordering sample pickup and discarding and execution of work orders.
May represent the department during regulatory inspections (or internal and external audits).
Provides input into scheduling of assignments by the team lead / manager.
Perform data verification and review
Records performance metrics
May update QC documents for managerial review and approval.
May lead simple projects within the team. Also contributes to complex projects.
May train colleagues in the execution of tasks and testing
Contributes to change controls
Supports deviation investigations and laboratory investigations through data gathering or interview process. May lead no impact deviations.
Identifies and escalates challenges & barriers to execution suggests solutions and participates in remediation.
Identifies and escalates method and/or instrument issues. Also supports and may lead solutions.
Positive supportive and actively collaborates within the team.
Actively and positively learns and participates in Operational Excellence (OpEx) and Continuous Improvement (CI) initiatives in the team.
Complete all required tasks compliantly and safely while consistently and intentionally modeling BMS values (Integrity Accountability Passion Urgency Innovation and Inclusion).
Perform other tasks as assigned.
Key Job Competencies
Ability to understand and follow procedures.
Ability to work in a fast-paced team environment meet deadlines and prioritize work.
Ability to communicate effectively with peers and management regarding task completion roadblocks and needs.
Attention to detail and demonstrate organizational skills.
Ability to manage multiple assignments while meeting timelines.
Knowledge of basic electronic systems (email MS Office etc.) and lab data systems (e.g. LIMS) required
Ability to interpret and apply cGMPs Compendia regulatory requirements and industry best practices.
Excellent organizational and critical thinking skills.
Is considered a fully independent analyst capable of executing tasks with no supervision
Problem-solving ability/mentality technically adept and logical.
Ability to write technical documents.
Qualifications & Experience
Key Job Competencies
Ability to understand and follow procedures.
Ability to work in a fast-paced team environment meet deadlines and prioritize work.
Ability to communicate effectively with peers and management regarding task completion roadblocks and needs.
Attention to detail and demonstrate organizational skills.
Ability to manage multiple assignments while meeting timelines.
Knowledge of basic electronic systems (email MS Office etc.) and lab data systems (e.g. LIMS) required
Ability to interpret and apply cGMPs Compendia regulatory requirements and industry best practices.
Excellent organizational and critical thinking skills.
Is considered a fully independent analyst capable of executing tasks with no supervision
Problem-solving ability/mentality technically adept and logical.
Ability to write technical documents.
Role Specific Assignments:
Manage QMS Records: Ensure all Quality Management System (QMS) records are maintained and updated in accordance with established procedures and regulatory requirements.
Support Equipment Validation and Decommissioning: Assist in the validation and decommissioning of equipment ensuring all activities comply with regulatory stand-ards and company protocols.
Education:
Bachelors Degree in a Scientific or relevant technical area with 1 year experience
OR
Masters degree in a Scientific or relevant Technical area.
An equivalent combination of education and experience preferably in a regulated environment will be considered.
Working Conditions: Office environment
Exposure to hazards or disagreeable conditions:
Work Location: Manati Site 100% OnSite
Hours: Mon-Fri 8a-5pm
Paga: 26.78 p/h
Position Summary
The Specialist in this role will be responsible for executing routine testing of complex and non-complex methods on intermediate or finished products a environmental monitoring utility testing raw materials etc. as appropriate for the individual role. They will also support lab operations activities such as housekeeping as required.
Key Responsibilities
Executes routine testing of non-complex/compendial methods environmental monitoring utility testing raw materials etc. as appropriate for the individual role
Perform release/stability testing for complex and non-complex methods on intermediate or finished product
Perform activities to support lab operations such as housekeeping alarm acknowledgement reagent preparation inventory management material and reagent ordering sample pickup and discarding and execution of work orders.
May represent the department during regulatory inspections (or internal and external audits).
Provides input into scheduling of assignments by the team lead / manager.
Perform data verification and review
Records performance metrics
May update QC documents for managerial review and approval.
May lead simple projects within the team. Also contributes to complex projects.
May train colleagues in the execution of tasks and testing
Contributes to change controls
Supports deviation investigations and laboratory investigations through data gathering or interview process. May lead no impact deviations.
Identifies and escalates challenges & barriers to execution suggests solutions and participates in remediation.
Identifies and escalates method and/or instrument issues. Also supports and may lead solutions.
Positive supportive and actively collaborates within the team.
Actively and positively learns and participates in Operational Excellence (OpEx) and Continuous Improvement (CI) initiatives in the team.
Complete all required tasks compliantly and safely while consistently and intentionally modeling BMS values (Integrity Accountability Passion Urgency Innovation and Inclusion).
Perform other tasks as assigned.
Key Job Competencies
Ability to understand and follow procedures.
Ability to work in a fast-paced team environment meet deadlines and prioritize work.
Ability to communicate effectively with peers and management regarding task completion roadblocks and needs.
Attention to detail and demonstrate organizational skills.
Ability to manage multiple assignments while meeting timelines.
Knowledge of basic electronic systems (email MS Office etc.) and lab data systems (e.g. LIMS) required
Ability to interpret and apply cGMPs Compendia regulatory requirements and industry best practices.
Excellent organizational and critical thinking skills.
Is considered a fully independent analyst capable of executing tasks with no supervision
Problem-solving ability/mentality technically adept and logical.
Ability to write technical documents.
Qualifications & Experience
Key Job Competencies
Ability to understand and follow procedures.
Ability to work in a fast-paced team environment meet deadlines and prioritize work.
Ability to communicate effectively with peers and management regarding task completion roadblocks and needs.
Attention to detail and demonstrate organizational skills.
Ability to manage multiple assignments while meeting timelines.
Knowledge of basic electronic systems (email MS Office etc.) and lab data systems (e.g. LIMS) required
Ability to interpret and apply cGMPs Compendia regulatory requirements and industry best practices.
Excellent organizational and critical thinking skills.
Is considered a fully independent analyst capable of executing tasks with no supervision
Problem-solving ability/mentality technically adept and logical.
Ability to write technical documents.
Role Specific Assignments:
Manage QMS Records: Ensure all Quality Management System (QMS) records are maintained and updated in accordance with established procedures and regulatory requirements.
Support Equipment Validation and Decommissioning: Assist in the validation and decommissioning of equipment ensuring all activities comply with regulatory stand-ards and company protocols.
Education:
Bachelors Degree in a Scientific or relevant technical area with 1 year experience
OR
Masters degree in a Scientific or relevant Technical area.
An equivalent combination of education and experience preferably in a regulated environment will be considered.
Working Conditions: Office environment
Exposure to hazards or disagreeable conditions:
Required Experience:
IC
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