Employment Opportunities

Careers at Boston Analytical

Boston Analytical offers a stimulating work environment for highly educated, technically skilled people seeking fulfilling, long-term employment. In addition to competitive salaries and benefits, Boston Analytical offers robust training and development programs, and we encourage employees to broaden their skills through continuing education. If you’re looking for ample opportunities for professional growth and advancement, working alongside the industry’s best and brightest, Boston Analytical is the place to be.

Job Openings


You can be considered for future opportunities by emailing your résumé to .

Current job postings are posted below:

QC Chemists - All Levels

The Chemist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures.  Duties will include analysis of pharmaceutical products using HPLC, GC, Dissolution, AA, UV-Vis, Wet Chemical Analysis and Method Development.

Primary Duties and Responsibilities:

·         Prepares and analyzes products to determine chemical and physical properties.

·         Documents work in a clear and organized manner.

·         Follows all safety rules and regulations and conducts periodic safety audits.

·         Follows all cGMP rules and regulations.

·         Under close supervision confers with chemists and other client personnel regarding research, procedures performed, related results and prepares reports.

·         Under close supervision will be trained to become proficient at assigned tasks in order to become subject matter experts.

·         Performs routine data generation and problem solving with a minimal rework.

·         Works under close supervision to ensure all work performed is performed in compliance with standard operating procedures, good manufacturing practices, and the regulations of the Food and Drug Administration.

·         Ensures all work performed strictly adheres to Company, client and Pharmacopeial methodologies.

·         Performs system maintenance and calibrations to ensure equipment is operating with specified requirements.

·         Proper handling of hazardous waste in compliance with the Company and DES hazardous waste rules.

REQUIREMENTS & QUALIFICATIONS
Qualification include a Bachelor’s degree in Chemistry or a related science discipline is required with 0-3 years of related experience. Knowledge of cGMPs and related compliance regulations and guidances is preferred.

MINIMUM SKILLS REQUIREMENTS

·         Must have the ability and skill to perform the detailed job requirements noted above competently, safely and proficiently. 

·         A self-starter, motivated person who possesses good interpersonal skills capable of effectively interacting with all departments and client personnel.

·         Must have excellent organizational, verbal communication and technical documentation skills.

·         Solid computer skills.

·         Knowledge of safe laboratory practices, including the proper procedures in handling chemicals and samples.

·         Must be a team player with integrity and concern for the quality of Company products, services and staff members.

 

 

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Systems Administrator

In this position you plan and coordinate the ongoing support and maintenance of Boston Analytical’s network infrastructure. Demonstrates strong subject matter knowledge pertaining to both IT capabilities and functional business processes, with particular strength in respect client relations.  In this role you are responsible for understanding overall goals and objectives of the business and assisting in the identification and delivery of technical and business process solutions and continuous improvement initiatives.

PRIMARY DUTIES AND RESPONISIBITIES

·         Provide first level and-user technical support including desktop and phones.

·         Provide exceptional customer service to internal employees.

·         Troubleshoot problems with network connectivity, web access and basic network connectivity and google access.

·         Resolve issues using appropriate troubleshooting and helpdesk ticketing.

·         Diagnose and resolve client side hardware problems or failures?

·         Oversee provision accounts for new users/terminated users as well as password administration.

·         Enforce company IT standards and IT policies.

·         Identify security risk to the environment from a client-side standpoint.

·         Manage and troubleshoot video conferencing systems.

·         Maintain software and hardware inventory.

·         Create and maintain IT related documents, procedures, and SOP’s.

·         Maintain and monitor IP Phone systems.

·         Provide advanced support for business applications including LIMS v6, Atlas 8.2, and Empower3.

REQUIREMENTS & QUALIFICATIONS

Qualification include a bachelor’s degree in computer science or related field with a minimum of 2+ years of relatable experience working with computers.

MINIMUM SKILLS REQUIREMENTS

·         Must have the ability and skill to perform the detailed job requirements noted above competently, safely and proficiently. 

·         A self-starter, motivated person who possesses good interpersonal skills capable of effectively interacting with all departments and client personnel.

·         A team player with the ability to seek direction or act independently as the situation demands.

·         Must be a team player with integrity and concern for the quality of Company products, services and staff members.

 

·         Experience with Empower, Labware LIMS, or Atlas 8.2 is a plus.

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Senior Scientist - ICP-MS

The Senior Scientist will perform analytical analysis of non-volatile compounds for the Raw Materials laboratory according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures.  Duties will include but not be limited to compendial analysis and method development of raw materials within the Raw Material Laboratory.  This position will report directly to the QC Director.

PRIMARY DUTIES AND RESPONSIBILITIES

·         Set-up, perform, and/or supervise analytical testing.

·         Prepares samples for analysis by ICP-MS. 

·         Analysis of sample solutions by ICP-MS to adequately resolve and identify all compounds. 

·         Coordinate ICP-MS findings with sample data from GC-MS and LC-MS analyses.

·         Author detailed cGMP reports outlining study findings.

·         Develop ICP-MS methods for drug product stability testing.

·         Performs system maintenance and calibrations to ensure equipment is operating with specified requirements. Ensures all work performed strictly adheres to Company, client and Pharmacopeial requirements.

·         Proper handling of hazardous waste in compliance with the Company and DES hazardous waste rules.

·         Confers with chemists and other client personnel regarding research, procedures performed and related results and prepares technical papers and reports.

·         As a subject matter expert, confers with Quality Assurance and Lab Management to design and/or improve standard operating procedures and/or training programs.

·         Provides over site to projects and assist other Analysts as needed.

·         Performs advanced data generation, analysis and solves complicated problem solving independently with minimal rework.

·         Reviews and assesses discrepancies; includes performing risk assessments, participating in root cause analysis investigations, tracking, follow-up and reporting.

·         Supervises, trains, and mentors other chemists on an as needed basis.

·         Documents work in a clear and organized manner.

·         Follows all safety rules and regulations and conducts periodic safety audits.

·         Follows all cGMP rules and regulations.

REQUIREMENTS & QUALIFICATIONS 

Qualifications include a minimum of a Master’s Degree in Analytical Chemistry with 8+ years’ experience. Strong knowledge of cGMPs and related compliance regulations and guidance required.

MINIMUM SKILLS REQUIREMENTS

·        Must have the ability and skill to perform the detailed job requirements noted above competently, safely and proficiently. 

·        A self-starter, motivated person who possesses good interpersonal skills capable of effectively interacting with all departments and client personnel.

·        Must have excellent organizational, verbal communication and technical documentation skills.

·        Must be a team player with integrity and concern for the quality of Company products, services and staff members.

·        Demonstrated ICP-MS operation and data interpretation capability.

·        Ability to develop and optimize HPLC and UPLC methods. 

·        Documented success managing complex projects to completion within customer expectations for deadline, cost, and overall deliverable.

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Technical Client Liaison

In this position you will interact on a daily basis with clients, sales and internal staff to ensure our clients' needs are being met. The goal is to provide outstanding customer service to our clients and to advocate for the client internally.

Primary Duties and Responsibilities

·         Communicate and define objectives and requirements necessary to structure the clients overall project.

·         Effectively communicate internally specific project needs of client.

·         Successfully manage projects and timelines to meet clients need and expectations.

·         Provide excellent communication skills to effectively communicate with the client by both phone and email.

·         Ability to follow internal processes for client requests, providing agendas and meeting minutes for conference calls, initiating new projects and assist in quote generation.

·         Requires professional conduct during conference calls, phone calls and email.

·         Responds in a timely fashion to all client inquiries.

·         Must understand client expectations and value of service to the client.

·         The successful candidate will be customer service focused and advocate for the clients’ needs. 

·         Daily review of incoming projects and interaction with sales staff.

·         Hold project kick off meetings internally and externally with clients.

Requirements:
Qualification include a BA or BS degree in Chemistry or Biology highly desired or Science related discipline. A minimum of 2-3 years in the pharmaceutical and/or medical device industry required. Knowledge of cGMPs and related compliance regulations and guidances a plus.

Minimum Skills Requirements:

·         Strong competencies in planning, project management, and organization with the ability to lead multiple activities while maintaining a focus on quality.

·         Must have excellent interpersonal, time management and organizational skills.

·         Be a team player but also skilled to work independently.

·         Detail oriented with the ability to follow-through in a timely manner.

·         Ability to multi-task and able to manage several projects at one time.

 

·         Must be motivated and have a positive attitude.

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Senior QC Chemist - Method Development and Method Validation

In this position the Senior Chemist will conduct quantitative and qualitative analyses of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures.  Duties will include analysis of pharmaceutical and related products using HPLCUPLC, GC, LC/MS, Dissolution, AA, UV-Vis, and Wet Chemical Analysis .  Method development and validation is also a major part of this role. In addition, the Senior Chemist will supervise, train and assist other Chemists on an as needed basis.

Primary Duties and Responsibilities:

  • Designs and develops experiments, processes, and methods for the solution of technical problems.  Able to work with a degree of independence.
  • Prepares and analyzes products to determine chemical and physical properties, identity, content and purity.
  • Conducts research on manufactured products to develop, improve and validate test procedures.
  • Troubleshoots instrument and confers with chemists and client personnel regarding research, procedures performed, related results, and prepares technical papers and reports.
  • Documents work in a clear and organized manner, with a high attention to detail.
  • Follows all safety rules and regulations and conducts periodic safety audits.
  • Ensures all appropriate work is performed in compliance with standard operating procedures, good manufacturing practices, and the regulations of the Food and Drug Administration and United States Pharmacopeia methodologies.
  • Performs system maintenance and calibrations to ensure equipment is operating with specified requirements.
  • Performs work at a level to be considered subject matter expert.  As subject matter expert, confers with Quality Assurance and Lab Management to design and/or improve standard operating procedures and/or training programs.

This position requires a MS or PhD degree in Analytical Chemistry or a related field with 5+ years of experience.  Knowledge of cGMP is a must.  Previous method development and validation experience required. Experience with LC/MS and Empower software extremely desirable.

Minimum Skills Requirements:

  • Knowledge of safe laboratory practices, including the proper procedures in handling chemicals and samples.
  • Strong oral and written communication skills
  • Strong organizational skills and attention to detail.
  • Ability to be an effective hands-on leader.
  • Method development and validation particularly in HPLC, LC/MS, UPLC and GC.
  • Dissolution, compendia chemistry methods for raw materials and Karl Fischer are a plus.
  • Familiarity with chromatography data systems, ELNs, and LIMS.

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Boston Analytical is an Equal Opportunity Employer.