employee relations manager salaries in boston, massachusetts

job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowledge in Oncology, Neuroscience, Rare Diseases, and Gastroenterology. As a company that brings in over $30 billion in annual revenue, they have established themselves as a biopharmaceutical powerhouse that is changing the world. If you're looking for a position where your work will benefit millions of people, we are waiting for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Lexington, Massachusetts job type: Contract salary: $40.00 - 53.39 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Primary Duties of this position will focus on the daily lab operations and execution of testing to support manufacturing operations /validation/or development studies. Testing may include but not limited to samples from drug substance and drug product manufacturing, stability and various protocol studies using approved test methods or test methods derived from QC technical protocols. May assist in sampling activities. This position is expected to maintain operational and GMP readiness of the QC areas as well as maintain critical reagent inventory such as antibodies and cell banks at business appropriate quantities. In addition, the individual may participate in more complex projects, operational excellence initiatives, and various quality systems with general supervision. Specific Biochemistry Focus Areas: Product Testing: Area focuses on techniques such as SDS-PAGE Silver, QPCR, Potency, Kinetics assay, Enzyme Activity, pH, Osmo, A280 etc., in order to support in-process, release and stability testing.Role supports commercial and clinical testing for defined site-based and external programs, as well as method transfer and validation. Introduction of new equipment and technology to improve sustainability and compliance is expected.Additionally, the role provides support for Quality projects and implementation of operational excellence initiatives. 40-50% Testing execution, participate in training analysts, trouble shooting of methods20-30%: QC operations support which entails data review, data trending, OE/5S/LEAN initiatives, maintenance of equipment and reagents, lab house keeping, support for other QC groups. Compliance and quality systems (SOP revisions, input to quality systems records)10-20% Involvement in various departmental and cross-functional teams and initiatives; inspection and regulatory support  qualifications: Typically requires a bachelor's degree and a minimum of 5+ years of related experience. (science related degree is preferred)Excellent communication, interpersonal and organizational skills.Ability to work well both independently and in a team environment.Ability to prioritize work and multitask.Previous experience in a GMP QC role is preferredKey Skills, Abilities, and CompetenciesDescribe critical skill and abilities needed to successfully perform the job, which should be representative of the knowledge, skills, and abilities required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.Complete understanding and application principles, concepts, practices and standards. Full knowledge of industry practices. Position requires critical thinking.Key Skills: MS Office, LIMS, SAP, Trackwise , compliance and strong science understandingLimited to no travel expected. Travel between sites is required.The following physical abilities are required in order to fulfill the job duties: Repetitive bending and reaching to setup and break-down equipment (if required by specific activity)Ability to work around chemicals (if working around the laboratories)Ability to wear personal protective equipment such as gloves, gowning, and respiratory protection in some casesAbility to walk and stand for periods of timeIndividual may be required to participate in environmental chamber monitoring program which would include the use of an on-call mobile phone as well as on-site support during non-business hours   skills: Quality control, GMP (Good Manufacturing Practice), LIMS (Laboratory Information Management System Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility). This posting is open for thirty (30) days.

Randstad is partnered with a reputable insurance company to fill a permanent position on their team managing their personal lines. This person will be responsible for managing existing business on secured accounts. This role involves a base salary along with commission and bonus potential. The role requires experience in insurance/personal lines. License preferred but not required. This role requires experience and knowledge within personal lines insurance. Qualifications: -Experience in personal lines account manager or client services -Excellent communication skillssalary: $58,000 - $60,000 per yearshift: Firstwork hours: 8 AM - 4 PMeducation: BachelorsResponsibilities-Manage existing book of business for personal lines customers -Make updates to existing policies, provide quotes for new policies -Process applications for any new policies -Review and process any/all policy renewals -Prepare any documenst related to Personal lines as needed -Handle requests for changes to policies or policy cancellationsSkillsAccount ManagementPersonal Lines (2 years of experience is required)Insurance (2 years of experience is required)Business operationsQualificationsYears of experience: 2 yearsExperience level: ExperiencedRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).This posting is open for thirty (30) days.

job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you!   location: Norwood, Massachusetts job type: Contract salary: $30.00 - 38.48 per hour work hours: 9 to 5 education: Bachelors   responsibilities: In this role, you will support cGMP microbiology methods for QC raw material, plasmid, drug substance, Stability and finished product testing for mRNA products produced at the company's manufacturing facility. This individual will contribute to non-testing projects and activities as needed example document certification, monthly biosafety cabinet cleaning etc. Execute compendial microbiological testing, and other methodologies as needed.Receive Environmental Monitoring Plates into MODA, Incubate, Microbial identification,Support testing for in-process samples, drug substance and drug product, including generation of testing data to support clinical studies.Assist in enumeration of test plates, review EM data, etc.Perform general laboratory support activities including reagent preparation, equipment maintenance, weekly and monthly cleaning of the BSCs, Document Certification, archival etc.Stock and perform inventory of lab supplies.Establish and maintain a safe laboratory working environment. Additional duties as may be assigned from time to time  qualifications: BS in a relevant scientific discipline with a minimum of 0 - 2 years (or MS in a relevant scientific discipline with 1 year) Quality Control experience in a cGMP organization Excellent troubleshooting and ability to communicate issues in a scientifically sound and understandable way.Familiarity with electronic databases (e.g. LIMS, SAP, LMS, or equivalent software)Strong written and oral communication skills as well as organizational skillsAbility to prioritize, manage and complete multiple projects and tasks in a fast-paced environment efficiently and independently.Working knowledge of relevant and current FDA, EU, ICH guidelines and regulations.A desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative.  skills: Quality control, GMP (Good Manufacturing Practice), LIMS (Laboratory Information Management System Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility). This posting is open for thirty (30) days.