Position: QA Specialist/Technical writerDuration: Long-TermLocation: Baltimore, MD( On-Site)Specific Tasks, Duties and Responsibilities:A cents € cents Initiates Quality Records and conducts deviation investigations that meeting both Industry and client expectationsA cents € cents Develops executes and oversees CAPAsA cents € cents Technical leadership will be required to ensure that product and process understanding is sufficient to investigate deviations,that investigations are technically sound, meet quality expectations, and that corrective actions are effective.A cents € cents Supports Tech transfer and process monitoring support as neededA cents € cents Works with the team to monitor critical process parametersA cents € cents Revision and management of manufacturing documents such as Batch Records and SOPsA cents € cents Leads or supports Continuous Improvement projectsA cents € cents Conducts data gathering, trending, and data presentation as needed to support investigationsA cents € cents Responsible for real-time, on the floor response in support of operational deviations by gathering information and completing an initial event report.A cents € cents Leads or manage investigations including root cause analysis and assesses product impact using input from various departmentsKnowledge/Skills Requirements:A cents € cents Previous experience in process deviation investigations and remediationA cents € cents Previous experience authoring and/or revising technical documentsA cents € cents Demonstrated ability to work effectively cross-functionallyA cents € cents Excellent communication and technical writing skillsA cents € cents Ability to support and/or lead system troubleshooting effortsA cents € cents Familiar with Lean Six Sigma Methodologies and proven analytical/problem-solving capabilitiesA cents € cents Ability to "get the job done"A' and take responsibility for results without direct authority; ability to coordinate, facilitate and organize resources.A cents € cents Superior customer service orientation with strong follow-up skills and attention to detail.A cents € cents Advanced PC skills, knowledge of company-specific software packagesA cents € cents Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, financial reports and legal documents.A cents € cents Demonstrated ability to read, write, and speak clearA cents € cents Experience using TrackwiseExperience:A cents € cents 5+ years of demonstrated technical competency in biopharmaceutical manufacturing processing in a GMP compliance environment(eg Production, Development, Process Engineering, Technical Services or related field)Job Type: ContractSalary: From $40.00 per hourSchedule:* 5x8* 8 hour shiftPeople with a criminal record are encouraged to applyAbility to commute/relocate:* Baltimore, MD 21218: Reliably commute or planning to relocate before starting work (Required)Experience:* Pharmacutical: 5 years (Required)Work Location: One location*Speak with the employer*+91 +1571-685-2793