Biopharmaceutical Associate I at GSK

, Maryland, United States -

Full Time

Start Date

Immediate

Expiry Date

23 May, 26

Salary

0.0

Posted On

22 Feb, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Media Preparation, Sterilization, Filtration, Equipment Operation, Sampling Procedures, Filter Integrity Testing, Process Monitoring, SOP Adherence, Documentation Compliance, Safety Policy Adherence, ERP Processes, Continuous Improvement, Automation Management, Digital Platforms, Microsoft Office, cGMP Knowledge

Industry

Pharmaceutical Manufacturing

Description

Nazwa biura: USA - Maryland - Rockville Posted Date: Feb 19 2026 The Rockville Biopharm site exists to produce and deliver biopharmaceutical drug substance of the highest quality in a safe, compliant, reliable and cost-effective manner for our patients. Our vision is to be wholly entrusted to make innovative, high quality medicines by leveraging the best talent and technology, on a platform of continuous improvement, to supply every patient, every time. This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: Key Responsibilities: Preparation, cleaning, sterilization, batching, pasteurization or filtration, and delivery of media and solutions for cell culture and purification operations. Perform the set-up, operation, cleaning, and break down of process equipment. Perform sampling procedures on various analytical instruments to analyze cell culture, solution, and/or product concentration characteristics. Operate Filter integrity devices to confirm the integrity of filters pre and post use. Perform process operations, equipment, and instrument monitoring and trending to enable proactive identification of issues to escalate and correct with applicable departments. Set-up of fixed and mobile process equipment and parts with CIP skids to carry out validated cleaning and sterilization processes. Follow appropriate standard operating procedures (SOPs), protocols, and batch records/logbooks to safely perform process operations and document compliantly with good documentation and data integrity practices. Follow all related safety policies and procedures and put safety first by playing an active role in identifying and correcting unsafe behaviors and conditions. Ability to choose a type of communication that is most effective in each situation. Knowledge and application of standard ERP processes in M-ERP following global and local procedures. Understanding of the GSK Production System (GPS) continuous improvement system and apply the GPS mindsets and behaviors. Knowledge and skill required to manage and use automation and emerging digital platforms. General knowledge of Microsoft Office Applications (Excel, Word, and Outlook). Additional Responsibilities for Higher Grades (BMA II, Sr. BMA and Lead BMA): Expertise and functional knowledge of the above areas with minimal guidance and producing quality results. Ability to articulate production equipment and/or manufacturing process problems to ensure accurate and detailed communication. Lead in the application of the GSK Production System (GPS) continuous improvement system and apply the GPS mindsets and behaviors in problem-solving. Assist resolution of technical and process problems; Identify, develop, and implement process improvements. Transfers information to audiences of varying levels of technical knowledge, so that each member of the audience clearly understands the message. Build positive relationships with others and conduct negotiation to establish win/win solutions. Developing team capability to learn with knowledge of coaching styles, listening and questioning techniques, feedback models, and emotional intelligence. An appreciation of cultural differences and diversity in the workplace. Why you? Basic Qualifications: We are looking for professionals with these required skills to achieve our goals: High School Diploma or GED Ability to work shifts that cover a 24/7 production operation. Ability to lift and carry materials up to 50 lbs. Ability to work in a clean environment adhering to all cleanliness standards established at site The selected candidate will be considered at the appropriate level based on experience 1+ years of directly related manufacturing experience in the pharmaceutical or biotechnology industry (BMA II) 3+ years of directly related manufacturing experience in the pharmaceutical or biotechnology industry (Sr. BMA) 5+ years of directly related manufacturing experience in the pharmaceutical or biotechnology industry (Lead BMA) Preferred Qualifications: If you have the following characteristics, it would be a plus: Bachelor of Science, Bachelor of Art, or Associate’s degree in biological sciences, chemical sciences, engineering, or equivalent technical discipline. Must be able to follow detailed processing instructions as well as accurately documenting any necessary information. Demonstrated ability to work effectively in a team. Ability to speak, read, write, and understand English. Strong verbal and written skills. Understanding of the basic Federal Drug Administration (FDA) and current Good Manufacturing Practices (cGMP) regulations #earlycareers • If you are based in Cambridge, MA; Waltham, MA; Rockville, MD; or San Francisco, CA, the annual base salary for new hires in this position ranges $19 to $32. The US salary ranges take into account a number of factors including work location within the US market, the candidate’s skills, experience, education level and the market rate for the role. In addition, this position offers an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. Available benefits include health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave. If salary ranges are not displayed in the job posting for a specific country, the relevant compensation will be discussed during the recruitment process. Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees. Why GSK? Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale. People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people. Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at HR.AmericasSC-CS@gsk.com where you can also request a call. Please note should your inquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a Recruitment FAQ guide. Click the link where you will find answers to multiple questions we receive GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/

Responsibilities

Key responsibilities involve the preparation, cleaning, sterilization, and delivery of media and solutions, alongside performing set-up, operation, and cleaning of process equipment for biopharmaceutical drug substance production. This role also includes performing sampling, operating filter integrity devices, and monitoring processes to proactively identify and escalate issues.