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2. B.A. or B.S. in Biochemistry, Biology, Chemistry, or related science. Able to perform analytical
work according to established Standard Operating Procedures. Analyze samples for metabolites,
turbidity, cell count and viability. Perform and report detailed Biophysical Characterization studies
utilizing FTIR, CD, SEC-MALS, UV-VIS, DLS, Fluorescence and SV-AUC in a leading Contract
Research Organization. PC skills and ability to learn new software and systems. Express, test and
rank enzyme variants in both HTP and shake flask scales. Protein purification utilizing IMAC, ion
exchange, affinity and size exclusion chromatography. Experience with capillary electrophoresis for
IEF, SDS-PAGE, and carbohydrate analysis preferred. Practical application of physical chemistry of
solids, suspensions, and colloids in an operations environment. Experienced in the operation of
multiple analytical instruments. Provide technical support to run and validate necessary test methods
on lab equipment and later perform product testing under cGMP. Experience transferring and
executing analytical assays in a biologics industry laboratory. Advanced degree preferred: Medical
Technology, Biology, Chemistry, Biochemistry. Effective team work, networking and ability to take
initiative. Support the development of critical reagents for a regulated diagnostics industry, utilizing
and authoring strong procedures, meeting quality system requirements. Analyze data and utilize a
LIMS system to track samples and analyses. Use scientific literature and database resources in the
execution of project related work. Performed hands-on wet chemistry techniques to support assay
development activities Prepare samples and perform analyses using automated. Experience in
velocity or equilibrium sedimentation methods. Prior quality control or laboratory experience in a
regulated industry environment. Performed biochemical testing on proteins and antibodies including,
but not limited to, CE, HPLC, SEC, and UV. Relevant work experiences may include: Diagnostics
method development or manufacturing, process validation or quality control. The primary duties of
the position will be purification and characterization of various recombinant protein targets. Writes
compliance documentation associated with investigations, data analyses, and experimental
conclusions. Evaluate and implement new technologies to embed the use of enzymes and synthetic
biology in new pharmaceutical manufacturing processes. At least six years related laboratory
experience including experience with biological testing on raw materials. Detail-oriented with strong
skills in multi-tasking and efficient management of day-to-day office operations. Maintain good a
good laboratory, documentation, and manufacturing practices. Use QLIMS and SAP as a tool to
track laboratory reagents, samples, and testing data. Cleaning, re-building, and sterilizing bioreactors
and other cell culture associated equipment.

3. Strong protein biochemistry and analytical skills with first hand knowledge in protein
characterization. Anticipating needs and maintaining right lab infrastructure. Assists with preparing
computer generated validation documents needed to accomplish routine technical assignments. May
lead a team or directly investigate the performance of manufacturing processes. Identifies and
initiates continuous improvement activities in line within the Siemens Production System (SPS)
framework. Exercise sound judgment in making decisions and the ability to work as a team player.
Working knowledge of clinical chemistry and application of automated assays in clinical chemistry
laboratories. Ability to objectively, accurately, and thoroughly convey complex issues in writing.
Coordinates and carries out investigations and implements corrective and preventive actions.
Maintain product reference and assay control programs. Skills: Numerical, Analytic and practical
Communication, Management Skills. Conduct and documents routine compendial, analytical testing
for in-process, release samples per SOP. Support the development of critical reagents for a regulated
diagnostics industry, utilizing and authoring strong procedures, meeting quality system requirements.
Additional backgrounds may include: Inorganic Chemistry, Physical Chemistry, Chemical
Engineering, Mathematics, Biochemical systems, and immunology. Knowledge of analytical methods
including: HPLC-Based Methods; Gel-Based Methods; CE-Based Methods; Cell-Based Assays;
Compendial Assays. Demonstrates a good grasp of knowledge and principles of field of
specialization and applies through successful completion of assignments. Apply scientific and
statistical principles and provide technical leadership to perform a wide variety of technical
investigations arising out of reagent performance issues encountered during reagent manufacturing.
Work primarily on ELISA based Assays (manual and automated). Served as a technician; purified
enzymes by FPLC and column chromatography; held responsibility for enzyme purification and
characterization; gained. Train new analysts for compendia and other analytical test methods per
training plans as needed. Participate and check workload scheduling and prioritization of staff to
ensure documents are reviewed and testing is performed in a timely manner. B.S degree in
biochemistry, biology, pharmaceutical sciences, or equivalent training with a minimum of 6 years
post degree experience in a relevant field of research, preferably working with proteins or. Skills:
Bioinformatics, Microsoft Office, Management Skills, Communication Skills. He is also an expert in
developing and maintaining laboratory procedures and protocols. BS in Medical Technology,
Biology, Chemistry, Biochemistry, Immunology. Ability to learn new techniques, perform multiple
tasks simultaneously, keep accurate records, follow instructions, and comply with company policies.
Represents Standards Manufacturing in cross functional meetings including; design element teams,
planning and scheduling, and product troubleshooting projects. Including these skills can help a
biochemist stand out from other applicants and demonstrate their qualifications. We collected the
best tips from seasoned Biochemist - Check out their advice to not only make your writing process
easier but also increase your chances of creating a resume that piques the interest of prospective
employers. Ability to accurately convey technical and scientific issues to people with varying levels
of expertise.

4. The primary duties of the position will be purification and characterization of various recombinant
protein targets. Evaluate laboratory SOPs and recommend improvement opportunities to maintain
compliance with corporate and regulatory guidelines. Ability to work both independently and in a
team setting. Capability of experimental design and independent data analysis. Consistently received
commendations for adaptability to changing situations and priorities Skills: Lab Management,
Writing (Methods, Test Plans, SOPs. Contribute to Protein Science efforts in standard and high
throughput expression screening and characterization of various recombinant protein targets
including membrane proteins and multi-protein complexes to enable generation of high quality
proteins for screening and structure determination. Authorization to work in the United States
indefinitely without restriction or sponsorship. Plan and execute iterative improvements to the initial
designs by using data generated. Perform analytical testing of clinical stage biopharmaceutical
products in accordance with cGMP regulations. Must know how to operate, maintain, and
troubleshoot on analytical instruments. Level of understanding business needs through participation
in business meetings, networking. Make sure you put your best foot forward and land your next job
with the help of Resumaker.ai. Ready to use templates that will help your resume stand out to
recruiters Try Resumaker's professional resume builder now. Support process characterization, test
method validation, and continuous improvement in manufacturing environment. A team player, be
flexible and demonstrate the ability to switch priorities to meet business needs. Experienced in
setting up laboratory experiments and analyzing results. Work effectively to build productive
relationships with other functional groups within the company. Manufacture, support, and
troubleshooting of IVD products. Bachelor’s degree in science or other related degree concentration.
BS in Medical Technology, Biology, Chemistry, Biochemistry. The successful candidate must be
highly organized, motivated, work independently in a collaborative team-oriented setting, and have
strong analytical, organizational, and communication skills. Effective team work, networking and
ability to take initiative. To plan and execute assigned experiments that support research activities
and project goals within the Enzyme Development team. Advanced degree MAY be substituted for
experience, where applicable. Manufacture, support, and troubleshooting of commercial and new
products. B.S. or B.A. in Biology, Molecular Biology, Microbiology, Biochemistry. Works in the
laboratory running Centaur family of instruments and Atellica instrument with serum and other
biological fluids of human and animal origin. Creates and participates in the design of experiments
(DOE) to troubleshoot manufacturing issues. Participates in conducting semi-complex tests or
investigations pertaining to the development of new designs methods, materials, or processes and
investigates possible application of results. Demonstrated experience in the analysis of therapeutic
proteins with at least one of the following: HPLC-Based Methods; Gel-Based Methods; CE-Based
Methods; Cell-Based Assays; Compendial Assays. Effectively uses fundamental concepts, practices,
and procedures of particular area of specialization.

5. Performed laboratory tests of blood and body fluids to help the detection, diagnosis, and treatment
of disease. Works in the laboratory running Atellica, Centaur, and CP instrumentation with serum
and other biological fluids of human and animal origin. Bachelor degree in chemistry, biochemistry,
biotechnology, or a related subject with a minimum of 4 years of experience or Master degree with 2
or more years of relevant experience. Experience with protein expression, preferably at both shake
flask and microtiter scales. Protein purification utilizing IMAC, ion exchange, affinity and size
exclusion chromatography. Use office and instrumentation specific computer software. Gaining
alignment on vision and execution with other businesses. Ability to write concisely and speak and
write persuasively. Candidate must have excellent verbal, written and listening skills and be able to
present facts clearly and concisely to staff members at all levels of the organization. We will give you
tips and advice on how to highlight your unique skills, experiences, and qualifications in order to
help you stand out from the competition. Maintain customer focus, motivate self, and demonstrate a
high degree of urgency. Advanced degree MAY be substituted for experience, where applicable.
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Carousel Next What is Scribd. Developed an analytical SDS-PAGE assay to detect the
environmental degradation of B.t. Designed, developed, and fabricated custom equipment for the
production of commercial products (Quantum Dots, LSPR Assays, Diffraction Gratings. Conduct
and documents routine compendial, analytical testing for in-process, release samples per SOP.
Experience in static or dynamic light scattering methods. Responsible for the implementation of new
instruments, assays, and informatics systems. Detailed protocols and performed product verification
and validation testing. Cleaning, re-building, and sterilizing bioreactors and other cell culture
associated equipment. Good skills are expected in: computers, customary MS Office programs,
various types of communication tools, laboratory skills (operation, maintenance, and troubleshooting
of analytical instruments and chemistry processes). Experienced in working in an FDA regulated
environment. Experience transferring and executing analytical assays in a biologics industry
laboratory. Contribute to Protein Science efforts in standard and high throughput expression
screening and characterization of various recombinant protein targets including membrane proteins
and multi-protein complexes to enable generation of high quality proteins for screening and structure
determination. Relevant work experiences may include: Diagnostics method development or
manufacturing, process validation or quality control. Skills: Chemical Skills, Laboratory Skills,
Communication Skills. A strong work ethic, excellent written and communication skills, and the
ability to work as a project leader as well as independently. Technical focus should be in Biology,
Biochemical Engineering, Biochemistry, Chemistry or Chemical Engineering. Must be flexible and
demonstrate the ability to switch priorities to meet business needs. Applied knowledge in Colloid
Science, Formulation, and Ion-selective electrodes (ISE) is a plus. Perform experiments and manage
routine cell maintenance activities with careful attention to detail and documentation. Work
collaboratively across multiple disciplines, as well as provide strong scientific input.

6. CGMP, HPLC Chemistry, Protein Characterization, Regulated Environment. May assist with
investigation of the performance of raw materials to use in the manufacture process of the product.
Work with the rest of the Biochemistry subgroup to help identify and resolve technical challenges
during screening campaigns, including the optimization of biochemical assays and assay workflows.
Prepare and validate written standard procedures for robust and efficient manufacturing process,
troubleshoot performance and process deviations, and communicate results to peers and
management via standard written, oral, or visual means. You'll receive a real-time score as you edit,
helping you to optimize your skills, experience, and achievements for the role you want. Performed
calibration and preventive maintenance of analytical equipment. Provides support in preparing
reports, charts, graphs, and other documents. Elevates complex issues that could impact supply
chain. Produce written reports (e.g., SOP, OMC, client reports). Bachelor's Degree in Protein
Biochemistry or related field with more than two years of research experience or Master's degree in
Protein Biochemistry or related field is required. Biophysical techniques (CD, FTIR, DLS, SEC-
MALLS, SV-AUC, fluorescence, UV-Vis). Bachelor's Degree with 2 years of experience or Master's
Degree in Immunology, Pharmacology, Biochemistry or similar area. D with 0-2 years of laboratory
experience in Biochemistry, Molecular Biology, Chemistry or related science. Work closely with
other members of the Biochemistry subgroup to develop and meet large-scale screening timelines.
The successful candidate must be highly organized, motivated, work independently in a collaborative
team-oriented setting, and have strong analytical, organizational, and communication skills.
Manufacturing of critical reagents for a regulated diagnostics industry, utilizing and authoring strong
procedures, meeting quality system requirements. Lead role in assay development projects from
conception (sourcing raw materials) to completion (transfer to manufacturing and
commercialization). Prepare and participate to health authorities inspections and internal audits in his
or her area. Assesses results for applicability, validity and conformance to design specifications, and
prepares reports on work results. Relevant work experiences may include: In-vitro diagnostic or
pharmaceutical product manufacture. Skills: Chemical Skills, Laboratory Skills, Communication
Skills. Provides assistance in research, analysis, and experimentation for product and process
development of immunoassays. Relevant work experiences may include: Diagnostics method
development or manufacturing. Anticipating needs and maintaining right lab infrastructure.
Successfully applies knowledge of fundamental concepts, practices, and procedures of particular area
of specialization and applies them through successful completion of assignments. Support process
characterization, test method validation, and continuous improvement in manufacturing environment.
Evaluate and implement new technologies to embed the use of enzymes and synthetic biology in
new pharmaceutical manufacturing processes. Perform and validate biochemical analysis including,
but not limited to, ligand binding assays, protein analysis, 1-D and 2-D PAGE analysis, samples
preparation for mass spectrometry. Experience in experimental design, use of DOE and statistical
analysis software and SPC is a plus. Follow all relevant internal and external regulatory requirements.