talent acquisition specialist salaries in boston, massachusetts

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: South Boston, Massachusetts job type: Temporary salary: $22 - 23 per hour work hours: 9 to 5 education: High School   responsibilities: This role is responsible for executing manufacturing operations on site. Responsible for maintaining a clean and orderly work environment. Completes work in a timely manner and performs all tasks with emphasis on safety. Works collaboratively with Manufacturing, Engineering, Quality Assurance, and other functional experts to support all daily operational activities. Consults with management to resolve quality, production, and efficiency problems. Functions in conjunction with manager and functional experts on special department projects. Works with internal departments to ensure implementation, maintenance, and improvement of the quality management system. Performs the essential duties and responsibilities as listed in section below. Manufacture biologically derived medical devices in a clean room environment (must be willing and able to follow clean room dress code requirements).Accurately and completely fill out required documentation, following GDP GSOP requirementsMaintain compliance to cGMP/ISO systemsFollow batch processing per procedures and forms trained toOperate processing inspection equipmentMaintain inventories of materialsParticipate in process improvement and validation activitiesComplete and pass all training and re-training requirements on-timePerform general cleaning of the clean rooms and other manufacturing spacesPerform general maintenance tasks as requiredMust be comfortable in working with animal tissue (skin and/or biological fluid)Perform all tasks with the emphasis on safety - Be respective of a ZERO tolerance policyPerform all tasks safely and thoroughly in a timely mannerFollow SOP's, Work Instructions, and other company policies and instructions at all timesUse company provided PPE, manufacturing equipment, chemicals, and other equipment safely, responsibly, and compliantlyMaintain good attendance and scheduled work hoursMust be comfortable working with sharp rotary bladesMust be comfortable working in a cleanroom with required PPEMust be able to work in teams and assist site with additional tasks as requestedMust be able to have good vision and ability to read measurement instrumentation for inspectionMust be able to safely lift and place items up to 50-60lbs.Must be computer literate/Word/Excel, etc.  qualifications: The requirements listed below are representative of the knowledge, skill and/or ability required for his position. Minimum required education and experience: High School Diploma or equivalent with 0-2 years of experienceExcellent Attendance RecordAbility to read, write and understand EnglishComputer literacy is requiredAbility to work overtime as requiredReliable Transportation TOOLS AND EQUIPMENT USED Lyophilizers (freeze dryers), pH meters, thermometers, balances (scales), sonicators, mixers, drop indicator, slicer machines, scalpels, temperature recorders, sealing machines PHYSICAL REQUIREMENTS The physical requirements listed in this section include, but are not limited, to the motor/physical abilities and skills require of position in order to successfully undertake the essential duties and responsibilities of this position. In accordance with the Americans with Disabilities Act (ADA), reasonable accommodations may be made to empower individuals with disabilities to undertake the essential duties and responsibilities of the position. While undertaking the essential duties and responsibilities of the position, the employee must repeatedly sit, listen, speak and have the ability to move throughout all locations of the building. The employee is required to go to all areas of the company. The employee may be required to periodically lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus. Ability to travel via car, train and/or airplane to domestic and international locations as needed. ADVERSE WORKING CONDITIONS The adverse working conditions listed in this section include, but are not limited to, those environmental conditions to which the employee may be exposed while undertaking the essential duties and responsibilities of this position. Adverse exposure may result from the handling of hazardous and bio-hazardous materials that include, but are not limited to, flammable and corrosive liquids, compressed gases, sharps, and medical wastes.   skills: SOP, MS-WORD, MS-EXCEL, GMP (Good Manufacturing Practice) 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).

Schedule is 6:00 PM to 6:00 AM Mon-Wed during batch production and 6:00 AM – 4:30 PM Mon-Thurs during non-batch production. The objective of this position is to perform manufacturing operations required to produce pharmaceutical products in a timely manner compliant with cGMP, OSHA, and other regulatory requirements. Under the direction of the manufacturing manager and on-the-floor guidance of the team lead, the manufacturing technician II will become qualified and independently capable of performing all aspects of internal cold manufacturing operations.  Such operations include, but are not limited to, receipt and transfer of materials and components into the manufacturing unit operation, component and equipment cleaning and preparation, operation of automated manufacturing equipment with good aseptic technique, completion of production transactions within the ERP system, completion of paper-based production records and forms in accordance with GDP.  Equipment utilized by the manufacturing technician II includes parts washers, sterilizers, tanks and vessels, single-use assemblies, filter integrity testers, automated filling equipment, inspection and packaging equipment. salary: $25 - $32 per hourshift: Thirdwork hours: 6 PM - 6 AMeducation: High SchoolResponsibilities  Performs the material transfer, preparation, batching, filling, inspection and ancillary operations associated with the manufacture of pharmaceutical products. Demonstrates ability and willingness to receive direction and coaching from team lead and manager Able to work effectively and re-prioritize work activities in a dynamic manufacturing environment Enters, checks and reviews data for accuracy and completeness, independently. Interacts positively with team members to coordinate functions and maximize efficiency. Resolves routine manufacturing problems independently or by utilizing the appropriate technical group resource and problem solving techniques. Utilizes knowledge, experience, and group resources to make decisions regarding routine issues. Communicates effectively across departments. Communicates effectively in situations involving pressure. Demonstrates an understanding and strict compliance with standard operating procedures (SOPs) Demonstrates the ability to apply knowledge of the cGMP Regulations (Parts 210 and 211) to routine situations. Demonstrates knowledge and fundamental understanding of operating computer-controlled automated production equipment. Demonstrates knowledge of applicable software. Performs numerous tasks ranging from basic to complex functions. The essential functions of this role include:working up to 4 hrs of overtime per weekSkillsManufacturing (3 years of experience is required)GMP (2 years of experience is required)aseptic techniques (1 year of experience is preferred)Standard Operating Procedures (1 year of experience is preferred)Batch Records (1 year of experience is preferred)QualificationsYears of experience: 3 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).

DIRECT HIREOur Client, a pharmaceutical company manufacturing innovative diagnostics, therapeutics and artificial intelligence solutions is looking for an experienced professional in the Pharmaceutical Manufacturing industry.We offer job security + career advancement + great pay + benefits, and best of all is that you will have a job with purpose: improve people’s lives all over the world. APPLY NOW to be part of our team.Location: North Billerica, MA2nd Shift available:Non Production weeks: MO - THU, 2nd shift 4pm – 2:30amProduction weeks: 6pm - 6am (MO - WED), 4pm - 8pm (THU) w/flexibilityPay Rate: $90K - $110K based on experience and qualifications+ Benefits (3 weeks of vacation, Medical/Dental, 401k, 9 holidays, 4 floating holidaysWhat you will be doing: Providing supervision of operations associated with pharmaceutical product while ensuring that all operations comply with all GMP, OSHA and other regulatory requirements. Acting as the technical expert of his/her team, with knowledge required to maintain a high level of operational efficiency, lead troubleshooting activities, lead investigations, analyze process/equipment data, identify and implement process improvements.Coordinating materials, equipment, personnel, utilities and activities within his/her team, the first shift Supervisor and with partner organizations, in order to achieve production schedule.Ensuring goals and metrics, identifying deficiencies; creating and executing action plans to mitigate issues. The right candidate will have: B.S. in science, engineering, biochemistry or related discipline + 2 years of experience leading operational personnel in routine or project settings (5 years without Bachelor’s degree).Minimum of 2 years of experience in a pharmaceutical environment.Aptitude for engineering principles and manufacturing automation systems TO APPLY: Email Resume to: claudia.mendoza@randstadusa.com or TEXT at 954.354.3808If this job is not for you, feel free to refer a friendSkills PharmaceuticalManufacturingcGMPGMPpharmaceuticsSOPsupervisorbiotechnologybiologychemistryBiotechchemical engineeringbiochemistrybiomedicalbiochemicalModernamilliporemilliporesigmaVertexoasis pharmaceuticalsalnylamkiniksa pharmaceuticalstakedanovobioticnovartisparatekaegerionamylyxscpharmaceuticalszata pharmaceuticalscorbusarmstrong pharmaceuticals Randstad 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).