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:

Technical Client Liaison - Project Manager

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 & QUALIFICATIONS

Qualification include a BA or BS degree in Chemistry, Biology or related science discipline preferred. 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.

Apply Online Now


QC Chemist

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.

 

 

Apply Online Now


Quality Assurance Specialist

The Quality Assurance Specialist supports the QA Lead and the company’s quality program by auditing chemists analytical data, routine work, protocols and reports.


Primary Duties and Responsibilities:

·         Auditing chemists’ routine project folders for conformance to company and customer requirements.

·         Write, review and edit Standard Operating Procedures (SOP’s, Forms and Methods) and familiarity with internal SOPs.

·         Alternate contact person for QA questions relating to laboratory operations and client correspondences.

·         Work with area management on the writing, issuance and tracking of deviations and investigations for closure.

·         Perform and assist with GMP audits.

·         Review and approval of Standard Operating Procedures, Specifications, Deviation Reports, Change Controls, and supporting documentation.

·         Review laboratory protocols and reports for accuracy and compliance to cGMP’s, as applicable.

·         Review and approval of data for determining the disposition of GMP material (raw material, in-process, finished product, packaging, labeling and manufacturing components) and the review and approval of documents and data associated with the Stability Program.

·         Other assigned responsibilities as established by the Quality Assurance Lead.

Requirements & Qualifications:
Qualification include a Bachelor’s degree in a related science discipline with 0-3 years of QA experience, preferably in a pharmaceutical industry.  Experience in a regulated industry. Experience writing and reviewing SOPs, QC data and documentation. Knowledge of LIMS a plus. Strong familiarity with regulatory/compliance environment (cGMP, GLP) associated with biotechnological, parenteral drug manufacture and/or medical device production.

Minimum Skills Requirements:

·         Knowledge of GMPs related compliance regulations and guidances are required.

·         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, analytical, verbal communication and technical documentation skills.

·         Good computer skills, such as MS office software.

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

Apply Online Now


Project Estimator - Quote Generation

The Project Estimator is responsible for drafting client quotations and ensuring the quotes are completed correctly and in a timely fashion.  This will include entering information into the workflow system and assisting in coordinating efforts to maintain timelines.  This position reports to the Quote Group Manager. The Estimator’s responsibilities include, but are not limited to, the following:

PRIMARY DUTIES AND RESPONISIBITIES

·         Entering the appropriate and necessary information coming from service requests from multiple internal leads to initiate the quoting process.

·         Coordinating internally to ensure the quote request meet each quote deadline, whether a requiring a standard turn-around time, or a rushed turn-around time. 

·         Updating multiple reports to track progress of active requests.

·         Understanding and utilizing the USP, NF, EP, and JP general chapter testing monographs to create quotes.

·         Pricing individual tests and testing studies.

·         Understanding and creating quotes for projects that may require multiple steps and/or R&D work.

·         Ability to manage multiple tasks at one time, all to completion ontime.

·         Review completed quotes for clarity, consistency and defined standards.  

·         Ability to work well with others and help coordinate people’s work for a common goal. 

·         Great attention to detail to ensure that the quality of the quote output meets our clients’ expectations.

REQUIREMENTS & QUALIFICATIONS
A BS degree in a scientific discipline is required with 0-2 years of related work experience. Basic computer skills are required. Experience with cGMP is preferred.

MINIMUM SKILLS REQUIREMENTS
Must have the ability and skill to perform the detailed job requirements noted above competently, safely, accurately and proficiently.  Self-starting motivated person who possesses excellent time management, multi-tasking and organizational skills. Must have an ability to prioritize and complete tasks efficiently and have excellent interpersonal skills who is able to clearly communicate with the manager and other groups. Must be detail oriented. Must be a team player with integrity and concern for the quality of Company products.

Apply Online Now


QC Microbiologist

The QC Microbiologist 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 through compendial methods and client specific test protocols.

Primary Duties and Responsibilities:

·         Prepares and analyzes samples to determine microbiological quality through the following analyses:  Microbial enumeration methods, absence of specified microorganisms, endotoxin, and water quality analysis (bioburden, TOC, Conductivity).

·         Performs genetic analysis of microbial growth to determine Genus/Species of unknown isolates.

·         Collects Environmental Monitoring Samples onsite and offsite at client manufacturing sites.

·         Documents work in a clear and organized manner.

·         Revises procedures and ELNs under close supervision.

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

·         Follows all cGMP rules and regulations.

·         Under close supervision confers with Microbiologists 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 executed 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 include a BA or BS degree in Microbiology or related science discipline with 0-2 years of related experience is required.  Knowledge of cGMP and related compliance regulations and guidances is preferred. ​

Minimum Skills:

·         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.

Apply Online Now


Senior Scientist - Extractables & Leachables

The Senior Scientist will contribute to Extractables & Leachables studies performed at Boston Analytical to support client submissions.  The ideal candidate will have experience operating LC-MS systems for analysis of non-volatile organic extractables and leachables.  The senior scientist role is also expected to serve as study director for E&L studies, including drafting protocols and assembling data into final reports. 

PRIMARY DUTIES AND RESPONISIBITIES

• Prepares samples for analysis by LC-MS.  

• Analysis of sample solutions by LC-MS to adequately resolve and identify all compounds.  

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

• Author detailed cGMP reports outlining study findings.

• Develop LC-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 Pharmacopial requirements.

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

REQUIREMENTS & QUALIFICATIONS

Qualification include a Ph.D. in Analytical Chemistry with 4+ years’ experience performing and interpreting LC-MS analysis or Master’s degree and 8+ years’ experience. Knowledge of cGMPs and current E&L best practices 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 writing skills. 

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

• Demonstrated LC-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.

Apply Online Now


Boston Analytical is an Equal Opportunity Employer.